{{Rsnum
|rsid=7932775
|Gene=SLC22A12
|Chromosome=11
|position=64600390
|Orientation=plus
|GMAF=0.376
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC22A12
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 5.3 | 25.7 | 69.0
| HCB | 17.5 | 41.6 | 40.9
| JPT | 30.1 | 47.8 | 22.1
| YRI | 47.9 | 38.9 | 13.2
| ASW | 33.3 | 43.9 | 22.8
| CHB | 17.5 | 41.6 | 40.9
| CHD | 17.4 | 42.2 | 40.4
| GIH | 4.0 | 28.7 | 67.3
| LWK | 48.6 | 39.4 | 11.9
| MEX | 5.4 | 41.1 | 53.6
| MKK | 30.8 | 53.8 | 15.4
| TSI | 2.0 | 35.3 | 62.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=19833602
|Title=Multiple single nucleotide polymorphisms in the human urate transporter 1 (hURAT1) gene are associated with hyperuricemia in Han Chinese
}}

{{PMID|21154327}} [Association of the exon 8 and intron 8 polymorphisms of the human urate transporter 1 gene with primary hyperuricemia in Chinese Han population].

{{on chip | Illumina Human 1M}}