{{Rsnum
|rsid=1227756
|Gene=COL13A1
|Chromosome=10
|position=71588504
|Orientation=plus
|GMAF=0.3916
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 27.4 | 54.0 | 18.6
| HCB | 8.8 | 35.0 | 56.2
| JPT | 5.3 | 45.1 | 49.6
| YRI | 12.9 | 45.6 | 41.5
| ASW | 8.8 | 40.4 | 50.9
| CHB | 8.8 | 35.0 | 56.2
| CHD | 6.4 | 39.4 | 54.1
| GIH | 13.9 | 58.4 | 27.7
| LWK | 11.8 | 35.5 | 52.7
| MEX | 13.8 | 51.7 | 34.5
| MKK | 13.5 | 50.0 | 36.5
| TSI | 27.5 | 43.1 | 29.4
| 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=G
|Pval=2E-7
|OR=0.57
|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}}