{{Rsnum
|rsid=10174098
|Gene=ITGAV
|Chromosome=2
|position=186628015
|Orientation=plus
|GMAF=0.3586
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ITGAV
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 45.1 | 46.0 | 8.8
| HCB | 56.9 | 39.4 | 3.6
| JPT | 64.6 | 33.6 | 1.8
| YRI | 30.6 | 44.2 | 25.2
| ASW | 22.8 | 54.4 | 22.8
| CHB | 56.9 | 39.4 | 3.6
| CHD | 65.1 | 32.1 | 2.8
| GIH | 49.5 | 37.6 | 12.9
| LWK | 10.0 | 54.5 | 35.5
| MEX | 32.8 | 44.8 | 22.4
| MKK | 16.0 | 49.4 | 34.6
| TSI | 43.1 | 46.1 | 10.8
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19818132
|Title=The ITGAV rs3738919 variant and susceptibility to rheumatoid arthritis in four Caucasian sample sets
|OA=1
}}

{{PMID Auto
|PMID=21116829
|Title=A polymorphism in the integrin alphaV subunit gene affects the progression of primary biliary cirrhosis in Japanese patients.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}