{{Rsnum
|rsid=2499604
|Chromosome=1
|position=237940201
|Orientation=minus
|GMAF=0.4697
|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 | 23.0 | 46.9 | 30.1
| HCB | 25.5 | 53.3 | 21.2
| JPT | 24.8 | 48.7 | 26.5
| YRI | 51.7 | 40.8 | 7.5
| ASW | 54.4 | 31.6 | 14.0
| CHB | 25.5 | 53.3 | 21.2
| CHD | 30.6 | 48.1 | 21.3
| GIH | 35.6 | 40.6 | 23.8
| LWK | 66.4 | 30.0 | 3.6
| MEX | 12.1 | 48.3 | 39.7
| MKK | 44.9 | 45.5 | 9.6
| TSI | 20.6 | 43.1 | 36.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20708005
|Trait=None
|Title=Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease
|RiskAllele=A
|Pval=0.000002
|OR=0.39
|ORtxt=[NR] unit decrease
|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}}