Editing Genetic variation

{{Short description|Difference in DNA among individuals or populations}}
{{Evolutionary biology}}
'''Genetic variation''' is the difference in [[DNA]] among individuals<ref>{{Cite web|date=2017-06-05|title=What is genetic variation?|url=https://www.ebi.ac.uk/training/online/course/human-genetic-variation-i-introduction/what-genetic-variation|access-date=2019-04-03|website=EMBL-EBI Train online|language=en}}</ref> or the differences between populations among the same species.<ref name="Genetic Variation">{{Cite web|title=Genetic Variation|url=https://www.genome.gov/genetics-glossary/Genetic-Variation|access-date=2020-09-28|website=Genome.gov|language=en}}</ref>  The multiple sources of genetic variation include [[mutation]] and [[genetic recombination]].<ref>{{Cite book|last=Levinson|first=Gene |title=Rethinking evolution: the revolution that's hiding in plain sight|publisher=World Scientific|year=2020|isbn=9781786347268}}</ref>  Mutations are the ultimate sources of genetic variation, but other mechanisms, such as  [[genetic drift]], contribute to it, as well.<ref name="Genetic Variation" />
[[Image:wheat.gif|right|thumb]]
[[File: Darwin's finches.jpeg|thumb|Darwin's finches or Galapagos finches<ref>Darwin, 1845. Journal of researches into the natural history and geology of the countries visited during the voyage of H.M.S. ''Beagle ''round the world, under the Command of Capt. Fitz Roy, R.N. 2d edition.</ref>]]
[[File:Genetic Variation and Inheritance.svg|thumb|Parents have similar gene coding in this specific situation where they reproduce and variation in the offspring is seen. Offspring containing the variation also reproduce and passes down traits to their offspring.]]
== Among individuals within a population ==

Genetic variation can be identified at many levels. Identifying genetic variation is possible from observations of [[phenotype|phenotypic]] variation in either quantitative traits (traits that vary continuously and are coded for by many genes, e.g., leg length in dogs) or discrete traits (traits that fall into discrete categories and are coded for by one or a few genes, e.g., white, pink, or red petal color in certain flowers).{{cn|date=December 2021}}

Genetic variation can also be identified by examining variation at the level of enzymes using the process of protein electrophoresis.<ref>{{Cite web|url=https://www.yourgenome.org/facts/what-is-gel-electrophoresis|title=What is gel electrophoresis?}}</ref>  Polymorphic genes have more than one allele at each locus.  Half of the genes that code for enzymes in insects and plants may be polymorphic, whereas polymorphisms are less common among vertebrates.{{cn|date=December 2021}}

Ultimately, genetic variation is caused by variation in the order of bases in the [[nucleotide]]s in genes. New technology now allows scientists to directly sequence DNA, which has identified even more genetic variation than was previously detected by protein electrophoresis. Examination of DNA has shown genetic variation in both coding regions and in the noncoding intron region of genes.{{cn|date=December 2021}}

Genetic variation will result in phenotypic variation if variation in the order of nucleotides in the [[DNA sequence]] results in a difference in the order of [[amino acid]]s in proteins coded by that DNA sequence, and if the resultant differences in [[Peptide sequence|amino-acid sequence]] influence the shape, and thus the function of the enzyme.<ref>{{cite journal|last1=Pavlopoulos|first1=GA|last2=Oulas|first2=A|last3=Iacucci|first3=E|last4=Sifrim|first4=A|last5=Moreau|first5=Y|last6=Schneider|first6=R|last7=Aerts|first7=J|last8=Iliopoulos|first8=I|title=Unraveling genomic variation from next generation sequencing data.|journal=BioData Mining|date=25 July 2013|volume=6|issue=1|pages=13|doi=10.1186/1756-0381-6-13|pmid=23885890|pmc=3726446 |doi-access=free }}</ref>

== Between populations ==
Differences between populations resulting from geographic separation is known as geographic variation. [[Natural selection]], [[genetic drift]], and [[gene flow]] can all contribute to geographic variation.<ref>{{Cite book |last1=Ann Clark |first1=Mary |url=https://openstax.org/books/biology-2e/pages/19-2-population-genetics |title=Biology 2e |last2=Douglas |first2=Matthew |last3=Choi |first3=Jung |date=2018-03-28 |publisher=OpenStax |isbn=978-1-947172-52-4 |pages=476 |language=en}}</ref>

== Measurement ==
Genetic variation within a population is commonly measured as the percentage of polymorphic [[Locus (genetics)|gene loci]] or the percentage of gene loci in heterozygous individuals. The results can be very useful in understanding the process of adaption to the environment of each individual in the population.<ref>{{Cite web |title=The Variety of Genes in the Gene Pool Can Be Quantified within a Population {{!}} Learn Science at Scitable |url=https://www.nature.com/scitable/topicpage/the-variety-of-genes-in-the-gene-6526291/ |access-date=2022-07-15 |website=www.nature.com |language=en}}</ref>

== Sources ==
[[File:Coquina variation3.jpg|thumb|upright|A range of variability in the mussel ''Donax variabilis'']]

Random [[mutation]]s are the ultimate source of genetic variation. Mutations are likely to be rare, and most mutations are neutral or deleterious, but in some instances, the new alleles can be favored by natural selection.  [[Polyploidy]] is an example of chromosomal mutation. Polyploidy is a condition wherein organisms have three or more sets of genetic variation (3n or more).

Crossing over ([[genetic recombination]]) and random segregation during [[meiosis]] can result in the production of new [[allele]]s or new combinations of alleles. Furthermore, random fertilization also contributes to variation. Variation and recombination can be facilitated by [[transposable elements|transposable genetic elements]], [[endogenous retrovirus]]es, LINEs, SINEs, etc.{{cn|date=December 2021}} For a given genome of a multicellular organism, genetic variation may be acquired in somatic cells or inherited through the germline.

== Forms ==
Genetic variation can be divided into different forms according to the size and type of genomic variation underpinning genetic change.
Small-scale sequence variation (<1 kilobase, kb) includes [[base-pair substitution]] and  [[indels]].<ref name="scher">{{cite journal |author=Lars Feuk, Andrew R. Carson & Stephen W. Scherer |title=Structural variation in the human genome |journal=Nature Reviews Genetics |volume=7 |pages=85–97 |date=February 2006 |doi=10.1038/nrg1767 |pmid=16418744 |issue=2|s2cid=17255998 }}</ref>
Large-scale [[structural variation]] (>1 kb) can be either [[copy number variation]] ([[Deletion (genetics)|loss]] or [[Gene duplication|gain]]), or [[chromosomal rearrangement]] ([[Chromosomal translocation|translocation]], [[Chromosomal inversion|inversion]], or Segmental acquired [[uniparental disomy]]).<ref name="scher" /> Genetic variation and recombination by transposable elements and endogenous retroviruses sometimes is supplemented by a variety of persistent viruses and their defectives which generate genetic novelty in host genomes.
Numerical variation in whole [[chromosome]]s or [[genome]]s can be either [[polyploidy]] or [[aneuploidy]].

== Maintenance in populations ==
A variety of factors maintain genetic variation in populations. Potentially harmful recessive alleles can be hidden from selection in the [[zygosity|heterozygous]] individuals in populations of [[ploidy|diploid]] organisms (recessive alleles are only expressed in the less common [[zygosity|homozygous]] individuals). Natural selection can also maintain genetic variation in balanced polymorphisms. Balanced polymorphisms may occur when heterozygotes are favored or when selection is frequency dependent.

==RNA viruses==

A high mutation rate caused by the lack of a proofreading mechanism appears to be a major source of the genetic variation that contributes to RNA virus evolution.<ref name="Carrasco2017">{{Cite journal |doi=10.1093/ilar/ilx026 |doi-access=free |pmc=7108571 |pmid=28985316|title=Are RNA Viruses Candidate Agents for the Next Global Pandemic? A Review |year=2017 |last1=Carrasco-Hernandez |first1=R. |last2=Jácome |first2=Rodrigo |last3=López Vidal |first3=Yolanda |last4=Ponce De León |first4=Samuel |journal=Ilar Journal |volume=58 |issue=3 |pages=343–358 }}</ref>  Genetic recombination also has been shown to play a key role in generating the genetic variation that underlies RNA virus evolution.<ref name = Carrasco2017/>  Numerous RNA viruses are capable of [[genetic recombination]] when at least two viral [[genome]]s are present in the same host cell.<ref name = Barr2010>{{cite journal | vauthors = Barr JN, Fearns R | title = How RNA viruses maintain their genome integrity | journal = The Journal of General Virology | volume = 91 | issue = Pt 6 | pages = 1373–87 | date = June 2010 | pmid = 20335491 | doi = 10.1099/vir.0.020818-0 | doi-access = free }}</ref>  RNA recombination appears to be a major driving force in determining genome architecture and the course of viral evolution among ''[[Picornavirus|Picornaviridae]]'' ([[positive-sense single-stranded RNA virus|(+)ssRNA]]) (e.g. [[poliovirus]]).<ref name="pmid31540135">{{cite journal | vauthors = Muslin C, Mac Kain A, Bessaud M, Blondel B, Delpeyroux F | title = Recombination in Enteroviruses, a Multi-Step Modular Evolutionary Process | journal = Viruses | volume = 11 | issue = 9 | date = September 2019 | pages = 859 | pmid = 31540135 | pmc = 6784155 | doi = 10.3390/v11090859 | doi-access = free }}</ref> In the ''[[retrovirus|Retroviridae]]'' ((+)ssRNA)(e.g. [[HIV]]), damage in the RNA genome appears to be avoided during [[reverse transcriptase|reverse transcription]] by strand switching, a form of genetic recombination.<ref name="pmid1700865">{{cite journal | vauthors = Hu WS, Temin HM | title = Retroviral recombination and reverse transcription | journal = Science | volume = 250 | issue = 4985 | pages = 1227–33 | date = November 1990 | pmid = 1700865 | doi = 10.1126/science.1700865 | bibcode = 1990Sci...250.1227H }}</ref><ref name="pmid30307534">{{cite journal | vauthors = Rawson JM, Nikolaitchik OA, Keele BF, Pathak VK, Hu WS | title = Recombination is required for efficient HIV-1 replication and the maintenance of viral genome integrity | journal = Nucleic Acids Research | volume = 46 | issue = 20 | pages = 10535–45 | date = November 2018 | pmid = 30307534 | pmc = 6237782 | doi = 10.1093/nar/gky910 |doi-access=free}}</ref><ref name = Bernstein2018>{{cite journal | vauthors = Bernstein H, Bernstein C, Michod RE | title = Sex in microbial pathogens | journal = Infection, Genetics and Evolution | volume = 57 | pages = 8–25 | date = January 2018 | pmid = 29111273 | doi = 10.1016/j.meegid.2017.10.024 | doi-access = free | bibcode = 2018InfGE..57....8B }}</ref>  Recombination also occurs in the ''[[Coronaviridae]]'' ((+)ssRNA) (e.g. [[Severe acute respiratory syndrome|SARS]]).<ref name = Su2016>{{cite journal | vauthors = Su S, Wong G, Shi W, Liu J, Lai AC, Zhou J, Liu W, Bi Y, Gao GF | display-authors = 6 | title = Epidemiology, Genetic Recombination, and Pathogenesis of Coronaviruses | journal = Trends in Microbiology | volume = 24 | issue = 6 | pages = 490–502 | date = June 2016 | pmid = 27012512 | doi = 10.1016/j.tim.2016.03.003 | doi-access = free | pmc = 7125511 }}</ref>  Recombination in RNA viruses appears to be an adaptation for coping with genome damage.<ref name = Barr2010/>  Recombination can occur infrequently between animal viruses of the same species but of divergent lineages. The resulting recombinant viruses may sometimes cause an outbreak of infection in humans.<ref name = Su2016/>

== History of genetic variation ==
Evolutionary biologists are often concerned with genetic variation, a term which in modern times has come to refer to differences in DNA sequences among individuals. However, quantifying and understanding genetic variation has been a central aim of those interested in understanding the varied life on earth since long before the sequencing of the first full genome, and even before the discovery of DNA as the molecule responsible for heredity. 

While today's definition of genetic variation relies on contemporary molecular genetics, the idea of heritable variation was of central importance to those interested in the substance and development of life even before the writings of Charles Darwin. The concept of heritable variation—the presence of innate differences between life forms that are passed from parents to offspring, especially within categories such as species—does not rely on modern ideas of genetics, which were unavailable to 18th- and 19th-century minds.

=== Pre-Darwinian concepts of heritable variation ===
In the mid-1700s, [[Pierre Louis Maupertuis]], a French scholar now known primarily for his work in mathematics and physics, posited that while species have a true, original form, accidents during the development of nascent offspring could introduce variations that could accumulate over time.<ref name=":0">{{Cite book|last=Bowler|first=Peter J. |title=Evolution: the history of an idea|date=1989|publisher=University of California Press|isbn=0-520-06385-6|edition=Rev. |location=Berkeley|oclc=17841313}}</ref> In his 1750 ''Essaie de Cosmologie'', he proposed that the species we see today are only a small fraction of the many variations produced by "a blind destiny", and that many of these variations did not "conform" to their needs, thus did not survive.<ref>{{Cite journal|last=Glass|first=Bentley|date=1947|title=Maupertuis and the Beginnings of Genetics |journal=The Quarterly Review of Biology|volume=22|issue=3|pages=196–210|doi=10.1086/395787|pmid=20264553|s2cid=28185536|issn=0033-5770}}</ref> In fact, some historians even suggest that his ideas anticipated the laws of inheritance further developed by [[Gregor Mendel]].<ref>{{Cite journal|last=Sandler|first=Iris|date=1983|title=Pierre Louis Moreau de Maupertuis: A precursor of Mendel? |journal=Journal of the History of Biology|volume=16|issue=1|pages=102|doi=10.1007/bf00186677|pmid=11611246|s2cid=26835071|issn=0022-5010}}</ref>

Simultaneously, French philosopher [[Denis diderot|Denis Diderot]] proposed a different framework for the generation of heritable variation. Diderot borrowed Maupertuis' idea that variation could be introduced during reproduction and the subsequent growth of offspring,<ref name=":1">{{Cite book|last=Gregory|first=Mary|doi=10.4324/9780203943823|title=Diderot and the Metamorphosis of Species|date=2006-10-23|publisher=Routledge|isbn=978-1-135-91583-4}}</ref> and thought that production of a "normal" organism was no more probable than production of a "monstrous" one.<ref>{{Cite journal|last=Hill|first=Emita|date=1968|title=Materialism and Monsters in "Le Rêve de d'Alembert"|jstor=40372379|journal=Diderot Studies|volume=10|pages=67–93|issn=0070-4806}}</ref> However, Diderot also believed that matter itself had lifelike properties and could self-assemble into structures with the potential for life.<ref name=":1" /> Diderot's ideas on biological transformation, introduced in his 1749 work [[Denis Diderot#Letter on the Blind|''Letter on the Blind'']], were thus focused on variability of spontaneously generated forms, not variability within existing species.<ref>{{Cite journal|last=Zirkle|first=Conway|date=1941|title=Natural Selection before the "Origin of Species"|jstor=984852|journal=Proceedings of the American Philosophical Society|volume=84|issue=1|pages=71–123|issn=0003-049X}}</ref>

Both Maupertuis and Diderot built on the ideas of  Roman poet and philosopher [[Lucretius]], who wrote in ''De rerum natura'' that all the universe was created by random chance, and only the beings that were not self-contradictory survived.<ref name=":2">{{Cite book|last=Gregory|first=Mary Efrosini |title=Evolutionism in eighteenth-century French thought|date=2008|publisher=Peter Lang|isbn=978-1-4331-0373-5|location=New York|oclc=235030545}}</ref> Maupertuis' work is distinguished from the work of both Lucretius and Diderot in his use of the concept of conformity in explaining differential survival of beings, a new idea among those who believed that life changed over time.<ref name=":2" />

Like Diderot, two other influential minds of the 18th century—[[Erasmus Darwin]] and [[Jean-Baptiste Lamarck]]—believed that only very simple organisms could be generated by spontaneous generation, so another mechanism was necessary to generate the great variability of complex life observed on earth.<ref name=":0" /> Erasmus Darwin proposed that changes acquired during an animal's life could be passed to its offspring, and that these changes seemed to be produced by the animal's endeavors to meet its basic needs.<ref>{{Cite journal|last=Zirkle|first=Conway|date=1946|title=The Early History of the Idea of the Inheritance of Acquired Characters and of Pangenesis|jstor=1005592|journal=Transactions of the American Philosophical Society|volume=35|issue=2|pages=91–151|doi=10.2307/1005592|issn=0065-9746}}</ref> Similarly, Lamarck's theory of the variability among living things was rooted in patterns of use and disuse, which he believed led to heritable physiological changes.<ref name=":0" /> Both Erasmus Darwin and Lamarck believed that variation, whether it arose during development or during the animal's life, was heritable, a key step in theories of change over time extending from individuals to populations.

In the subsequent century, [[William Herschel]]'s telescopic observations of diverse nebulae across the night sky suggested to him that different nebulae could each be in different stages in the process of condensation. This idea, which came to be known as the [[nebular hypothesis]], suggested that natural processes could both create order out of matter and introduce variation, and that these processes could be observed over time.<ref name=":0" />&nbsp;While it may seem to the modern reader that astronomical theories are irrelevant to theories of organic variation, these ideas became significantly conflated with ideas of biological transformation—what we now know as evolution—in the mid-19th century, laying important groundwork for the work of subsequent thinkers such as Charles Darwin.<ref>{{Cite journal|last=Schweber|first=S.S.|date=1989|title=John Herschel and Charles Darwin: A study in parallel lives |journal=Journal of the History of Biology|volume=22|issue=1|pages=1–71 |doi=10.1007/bf00209603|s2cid=122572397|issn=0022-5010}}</ref> 

=== Darwin's concept of heritable variation ===
[[Charles Darwin]]'s ideas of heritable variation were shaped by both his own scientific work and the ideas of his contemporaries and predecessors.<ref>{{Cite journal|last=Egerton|first=Frank N.|date=1976|title=Darwin's Early Reading of Lamarck|jstor=230686|journal=Isis|volume=67|issue=3|pages=452–456|doi=10.1086/351636|s2cid=144074540|issn=0021-1753}}</ref> Darwin ascribed heritable variation to many factors, but particularly emphasized environmental forces acting on the body. His theory of inheritance was rooted in the (now disproven) idea of [[Pangenesis|gemmules]] - small, hypothetical particles, which capture the essence of an organism and travel from all over the body to the reproductive organs, from which they are passed to offspring.<ref>{{Cite journal|last=Winther|first=Rasmus G.|date=2000|title=Darwin on Variation and Heredity|jstor=4331610|journal=Journal of the History of Biology|volume=33|issue=3|pages=425–455|doi=10.1023/A:1004834008068|s2cid=55795712|issn=0022-5010}}</ref> Darwin believed that the causal relationship between the environment and the body was so complex that the variation this relationship produced was inherently unpredictable.<ref>{{Cite journal|last=Beatty|first=John|date=2006-12-01|title=Chance Variation: Darwin on Orchids|journal=Philosophy of Science|volume=73|issue=5|pages=629–641|doi=10.1086/518332|s2cid=170396888|issn=0031-8248}}</ref> However, like Lamarck, he acknowledged that variability could also be introduced by patterns of use and disuse of organs.<ref name=":3">{{Cite journal|last=Deichmann|first=Ute|date=2010|title=Gemmules and Elements: On Darwin's and Mendel's Concepts and Methods in Heredity|jstor=20722529|journal=Journal for General Philosophy of Science|volume=41|issue=1|pages=85–112|doi=10.1007/s10838-010-9122-0|s2cid=42385140|issn=0925-4560}}</ref> Darwin was fascinated by variation in both natural and domesticated populations, and his realization that individuals in a population exhibited seemingly purposeless variation was largely driven by his experiences working with animal breeders.<ref>{{Cite journal|last=Bowler|first=Peter J.|date=2009-01-09|title=Darwin's Originality |journal=Science|volume=323|issue=5911|pages=223–226|doi=10.1126/science.1160332|pmid=19131623|s2cid=1170705|issn=0036-8075}}</ref> Darwin believed that species changed gradually, through the accumulation of small, continuous variations, a concept that would remain hotly contested into the 20th century.<ref name=":4">{{Cite book|last=Provine|first=William B. |title=The origins of theoretical population genetics|date=2001|publisher=University of Chicago Press|isbn=0-226-68463-6|edition=2nd |location=Chicago|oclc=46660910}}</ref>

=== Post-Darwinian concepts of heritable variation ===
In the 20th century, a field that came to be known as [[population genetics]] developed. This field seeks to understand and quantify genetic variation.<ref name=":4" /> The section below  consists of a timeline of selected developments in population genetics, with a focus on methods for quantifying genetic variation.

* '''1866''' - '''Heterozygosity''': Gregor Mendel's hybridization experiments introduced the concept that in the 1950s came to be recognized as [[Zygosity#Heterozygous|heterozygosity]].<ref name=":3" /> In a [[diploid]] species, one that contains two copies of DNA within each cell (one from each parent), an individual is said to be a heterozygote at a particular location in the genome if its two copies of DNA differ at that site. Heterozygosity, the average frequency of heterozygotes in a population, became a fundamental measure of the genetic variation in a population by the mid-20th century.<ref>{{Cite web|title=Heterozygosity|url=https://www.oxfordbibliographies.com/view/document/obo-9780199941728/obo-9780199941728-0039.xml|access-date=2021-12-11|website=Oxford Bibliographies |language=en}}</ref> If the heterozygosity of a population is zero, every individual is homozygous; that is, every individual has two copies of the same allele at the locus of interest and no genetic variation exists. 
* '''1918''' -  '''Variance''': In a seminal paper entitled "The correlation between relatives on the supposition of Mendelian inheritance", [[Ronald Fisher|R.A. Fisher]] introduced the statistical concept of [[variance]]; the average of squared deviations of a collection of observations from their mean (<math display="inline">\sigma^2=\frac{1}{I}\sum_{i=1}^I(x_i-\mu)^2</math>), where <math>\sigma^2</math> is the variance and <math>\mu</math> is the mean of the population from which the observations <math>x_i</math> are drawn).<ref name=":5">{{Cite journal|last1=Charlesworth|first1=Brian|last2=Edwards|first2=Anthony W. F.|date=2018-07-26|title=A century of variance |journal=Significance|volume=15|issue=4|pages=20–25|doi=10.1111/j.1740-9713.2018.01170.x |doi-access=free|issn=1740-9705}}</ref> R.A. Fisher's work in population genetics was not just important to population genetics; these ideas would also form the foundations of modern statistics.
* '''1918, 1921''' - '''Additive and dominant genetic variance''': R.A. Fisher subsequently subdivided his general definition of variance into two components relevant to population genetics: additive and dominant genetic variance.<ref>{{Cite journal|last=Dietrich|first=Michael|date=2013-01-01|title=R.A. Fisher and the Foundations of Statistical Biology|url=https://digitalcommons.dartmouth.edu/facoa/33|journal=Outsider Scientists: Routes to Innovation in Biology}}</ref> An additive genetic model assumes that genes do not interact if the number of the genes affecting the phenotype is small and that a trait value can be estimated simply by summing the effect of each gene on the trait. Under Fisher's model, the total genetic variance is the sum of the additive genetic variance (the variance in a trait due to these additive effects) and the dominant genetic variance (which accounts for interactions between genes).<ref name=":5" />
* '''1948''' - '''Entropy''': Unlike variance, which was developed with the purpose of quantifying genetic variance, [[Claude Shannon|Claude Shannon's]] measure of diversity, now known as [[Shannon entropy]], was developed as part of his work in communication theory as a way to quantify the amount of information contained in a message. However, the method quickly found use in population genetics, and was the central method used to quantify genetic diversity in a seminal paper by Richard Lewontin, "The Apportionment of Human Genetic Diversity".<ref>{{cite book |last=Rosenberg|first=Noah A.|chapter=Variance-Partitioning and Classification in Human Population Genetics|doi=10.1017/9781316276259.040 |editor=Rasmus Grønfeldt Winther |title=Phylogenetic Inference, Selection Theory, and History of Science|year=2018|pages=399–404|publisher=Cambridge University Press|isbn=9781316276259}}</ref>
* '''1951'' - ''F-statistics''': [[F-statistics]], also known as fixation indices, were developed by population geneticist [[Sewall Wright]] to quantify differences in genetic variation within and between populations. The most common of these statistics, F<sub>ST</sub>, considers in its simplest definition two different versions of a gene, or alleles, and two populations that contain one or both of these two alleles. F<sub>ST</sub> quantifies the genetic variability among these two populations by computing the average frequency of heterozygotes across the two populations relative to the frequency of heterozygotes if the two populations were pooled.<ref>{{Cite journal|last1=Alcala|first1=Nicolas|last2=Rosenberg|first2=Noah A|date=2017-07-01|title=Mathematical Constraints on FST: Biallelic Markers in Arbitrarily Many Populations|journal=Genetics|volume=206|issue=3|pages=1581–1600|doi=10.1534/genetics.116.199141 |pmid=28476869|pmc=5500152|doi-access=free|issn=1943-2631}}</ref> F-statistics introduced the idea of quantifying hierarchical concepts of variance and would become the foundation of many important population genetic methods, including a set of methods that tests for evidence of natural selection in the genome.<ref>{{Cite journal|last1=Excoffier|first1=L.|last2=Hofer|first2=T.|last3=Foll|first3=M.|date=October 2009 |title=Detecting loci under selection in a hierarchically structured population|journal=Heredity|language=en|volume=103|issue=4|pages=285–298|doi=10.1038/hdy.2009.74 |pmid=19623208|doi-access=free |issn=1365-2540}}</ref>

== See also ==
* [[Genetic diversity]]
* [[Genetic variability]]
* [[Human genetic variation]]
* [[Cheetah#Genetics]] - animal with known low genetic variability
* [[Population_bottleneck#Examples]]

== References ==
{{Reflist}}

== Further reading ==
* [[Ernst Mayr|Mayr E.]] (1970): Populations, species, and evolution – An abridgment of Animal species and evolution. The Belknap Press of Harvard University  Press, Cambridge, Massachusetts and London, England, {{ISBN|0-674-69013-3}}.
* [[Theodosius Dobzhansky|Dobzhansky T.]] (1970):  Genetics of the evolutionary process. Columbia,  New York, {{ISBN|0-231-02837-7}}.
*  McGinley, Mark; J. Emmett Duffy (ed). 2008. "[http://www.eoearth.org/article/Genetic_variation Genetic variation]." In: ''Encyclopedia of Earth''. Washington, D.C.: [[National Council for Science and the Environment]]. 
* [https://books.google.com/books?id=gIGyZHHmK98C&pg=PA7 "Genetic Variation"] in Griffiths, A.J.F. ''Modern Genetic Analysis, Vol 2.'', p.&nbsp;7
* [https://books.google.com/books?id=ANT8VB14oBUC&pg=PA456 "How is Genetic Variation Maintained in Populations"] in Sadava, D. et al. ''Life: The Science of Biology'', p.&nbsp;456
* [[Eviatar Nevo|Nevo, E.]]; Beiles, A. "[http://www.scholarpedia.org/article/Genetic_variation_in_nature Genetic variation in nature]". [[Scholarpedia]], 6(7):8821. [[doi:10.4249/scholarpedia.8821]]
* Hedrick P. (2011): Genetics of populations. Jones & Bartlett Learning, {{ISBN|978-0-7637-5737-3}}.
*{{cite journal | last=Albers | first=Patrick K. | last2=McVean | first2=Gil | title=Dating genomic variants and shared ancestry in population-scale sequencing data | journal=PLOS Biology | volume=18 | issue=1 | date=2020-01-17 | issn=1545-7885 | pmid=31951611 | pmc=6992231 | doi=10.1371/journal.pbio.3000586 | doi-access=free | page=e3000586|biorxiv=10.1101/416610
}}
* Rieger  R. Michaelis A.,  Green M. M.  (1976): Glossary of genetics and cytogenetics: Classical and molecular. Springer-Verlag, Heidelberg - New York, {{ISBN|3-540-07668-9}}; {{ISBN|0-387-07668-9}}.
* Griffiths, A. J. F. (1999). An Introduction to genetic analysis. W. H. Freeman, San Francisco, {{ISBN|0-7167-3520-2}}.
* [[Luigi Luca Cavalli-Sforza|Cavalli-Sforza L. L.]], Bodmer W. F. (1999): ''The genetics of human populations''. Dover, Mineola, New York, {{ISBN|0-486-40693-8}}.

==External links==
*[http://evolution.berkeley.edu/evolibrary/article/0_0_0/evo_17 Genetic variation]

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[[Category:Population genetics]]