{{Rsnum
|rsid=9333289
|Gene=ITGAV
|Chromosome=2
|position=186633380
|Orientation=plus
|GMAF=0.1827
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ITGAV
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.8 | 43.4 | 47.8
| HCB | 1.5 | 29.9 | 68.6
| JPT | 0.0 | 15.0 | 85.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 8.8 | 91.2
| CHB | 1.5 | 29.9 | 68.6
| CHD | 0.0 | 20.2 | 79.8
| GIH | 7.9 | 39.6 | 52.5
| LWK | 0.0 | 0.9 | 99.1
| MEX | 5.2 | 41.4 | 53.4
| MKK | 0.0 | 4.5 | 95.5
| TSI | 6.9 | 44.1 | 49.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=18694400
|Title=Integrin alpha V polymorphisms and haplotypes in a Korean population are associated with susceptibility to chronic hepatitis and hepatocellular carcinoma
}}

{{PMID|14681825|OA=1
}} Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}