{{Rsnum
|rsid=1305088
|Gene=SLC46A3
|Chromosome=13
|position=28704313
|Orientation=minus
|GMAF=0.202
|Gene_s=RNU6-53,SLC46A3
|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 | 0.0 | 14.2 | 85.8
| HCB | 10.9 | 43.1 | 46.0
| JPT | 6.2 | 43.4 | 50.4
| YRI | 16.3 | 45.6 | 38.1
| ASW | 14.0 | 35.1 | 50.9
| CHB | 10.9 | 43.1 | 46.0
| CHD | 13.8 | 56.0 | 30.3
| GIH | 5.0 | 31.7 | 63.4
| LWK | 12.7 | 51.8 | 35.5
| MEX | 0.0 | 19.0 | 81.0
| MKK | 3.8 | 44.9 | 51.3
| TSI | 1.0 | 4.9 | 94.1
| 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=0.000009
|OR=0.58
|ORtxt=[NR] unit increase
|OA=1
}}

{{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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}