{{Rsnum
|rsid=1354492
|Gene=ACCN1
|Chromosome=17
|position=33410403
|Orientation=minus
|GMAF=0.3985
|Gene_s=ASIC2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 15.3 | 49.5 | 35.1
| HCB | 1.5 | 18.7 | 79.9
| JPT | 0.0 | 20.5 | 79.5
| YRI | 46.6 | 44.5 | 8.9
| ASW | 44.6 | 42.9 | 12.5
| CHB | 1.5 | 18.7 | 79.9
| CHD | 0.0 | 18.5 | 81.5
| GIH | 19.0 | 42.0 | 39.0
| LWK | 31.8 | 51.4 | 16.8
| MEX | 14.0 | 56.1 | 29.8
| MKK | 11.6 | 50.3 | 38.1
| TSI | 26.3 | 48.5 | 25.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21810271
|Trait=None
|Title=Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.
|RiskAllele=A
|Pval=0.000002
|OR=0.1600
|ORtxt=[0.10-0.22] IU/dL increase
|OA=1
}}

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