{{Rsnum
|rsid=6717546
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=UGT1A10
|position=233773473
|Gene_s=UGT1A1,UGT1A3,UGT1A4,UGT1A5,UGT1A6,UGT1A7,UGT1A8,UGT1A9,UGT1A10
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 10.7 | 49.1 | 40.2
| HCB | 8.9 | 33.3 | 57.8
| JPT | 17.0 | 39.3 | 43.8
| YRI | 27.9 | 49.7 | 22.4
| ASW | 31.6 | 54.4 | 14.0
| CHB | 8.9 | 33.3 | 57.8
| CHD | 12.0 | 40.7 | 47.2
| GIH | 13.9 | 49.5 | 36.6
| LWK | 20.2 | 48.6 | 31.2
| MEX | 20.7 | 46.6 | 32.8
| MKK | 28.2 | 46.2 | 25.6
| TSI | 16.7 | 50.0 | 33.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=24822274
|Title=The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: haplotype associations and gene–environment interactions
}}

{{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}}