{{Rsnum
|rsid=3741414
|Gene=INHBC
|Chromosome=12
|position=57450266
|Orientation=minus
|GMAF=0.1506
|Gene_s=INHBC
|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 | 2.7 | 43.8 | 53.6
| HCB | 2.2 | 14.6 | 83.2
| JPT | 0.9 | 8.8 | 90.3
| YRI | 0.0 | 14.3 | 85.7
| ASW | 1.8 | 19.3 | 78.9
| CHB | 2.2 | 14.6 | 83.2
| CHD | 1.8 | 13.8 | 84.4
| GIH | 0.0 | 12.9 | 87.1
| LWK | 0.0 | 9.2 | 90.8
| MEX | 15.5 | 48.3 | 36.2
| MKK | 0.0 | 6.4 | 93.6
| TSI | 2.0 | 22.5 | 75.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23263486
  |Trait=Urate levels
  |Title=Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
  |RiskAllele=T
  |Pval=2E-25
  |OR=.07
  |ORtxt=[0.058-0.085] mg/dl decrease
  |OA=1
}}

{{PMID Auto
|PMID=24408252
|Title=The frequency of single nucleotide polymorphisms and their association with uric acid concentration based on data from genome-wide association studies in the Korean population
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}