{{Rsnum
|rsid=3800569
|Gene=ATP6V0A4
|Chromosome=7
|position=138726680
|Orientation=minus
|GMAF=0.2094
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ATP6V0A4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 54.0 | 35.4 | 10.6
| HCB | 60.6 | 37.2 | 2.2
| JPT | 61.9 | 34.5 | 3.5
| YRI | 81.0 | 17.7 | 1.4
| ASW | 54.4 | 43.9 | 1.8
| CHB | 60.6 | 37.2 | 2.2
| CHD | 52.3 | 41.3 | 6.4
| GIH | 65.3 | 31.7 | 3.0
| LWK | 80.9 | 18.2 | 0.9
| MEX | 72.4 | 27.6 | 0.0
| MKK | 87.1 | 12.3 | 0.6
| TSI | 49.0 | 44.1 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21326311
|Trait=None
|Title=Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients
|RiskAllele=C
|Pval=0.000006
|OR=1.2000
|ORtxt=[0.69-1.71] unit increase
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}