{{Rsnum
|rsid=1836127
|Gene=LOC643339
|Chromosome=12
|position=93156525
|Orientation=plus
|GMAF=0.3526
|Gene_s=OR2A41P
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 33.9 | 46.4 | 19.6
| HCB | 62.8 | 31.4 | 5.8
| JPT | 36.3 | 45.1 | 18.6
| YRI | 44.9 | 42.9 | 12.2
| ASW | 38.6 | 38.6 | 22.8
| CHB | 62.8 | 31.4 | 5.8
| CHD | 47.7 | 48.6 | 3.7
| GIH | 22.8 | 46.5 | 30.7
| LWK | 48.2 | 45.5 | 6.4
| MEX | 32.8 | 44.8 | 22.4
| MKK | 42.3 | 41.7 | 16.0
| TSI | 35.3 | 40.2 | 24.5
| 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=0.000003
|OR=0.76
|ORtxt=[NR] unit 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}}