{{Rsnum
|rsid=9310709
|Chromosome=3
|position=23052083
|Orientation=plus
|GMAF=0.416
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 24.8 | 50.4 | 24.8
| HCB | 22.6 | 38.7 | 38.7
| JPT | 22.1 | 42.5 | 35.4
| YRI | 2.0 | 26.5 | 71.4
| ASW | 3.5 | 33.3 | 63.2
| CHB | 22.6 | 38.7 | 38.7
| CHD | 25.7 | 52.3 | 22.0
| GIH | 27.7 | 48.5 | 23.8
| LWK | 1.8 | 34.5 | 63.6
| MEX | 44.8 | 46.6 | 8.6
| MKK | 9.6 | 33.3 | 57.1
| TSI | 20.6 | 55.9 | 23.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20686651
|Trait=None
|Title=Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases
|RiskAllele=C
|Pval=0.000002
|OR=1.15
|ORtxt=[1.09-1.22]
|OA=1
}}

This SNP is reportedly associated with [[chronic kidney disease]] and [[kidney stones]]. {{PMID|20686651|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}}