{{Rsnum
|rsid=3794260
|Gene=WSCD2
|Chromosome=12
|position=108204497
|Orientation=plus
|GMAF=0.04683
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=WSCD2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 1.8 | 98.2
| HCB | 2.2 | 26.3 | 71.5
| JPT | 3.5 | 27.4 | 69.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.2 | 26.3 | 71.5
| CHD | 0.0 | 20.2 | 79.8
| GIH | 1.0 | 16.8 | 82.2
| LWK | 0.0 | 4.6 | 95.4
| MEX | 0.0 | 3.5 | 96.5
| MKK | 0.0 | 3.8 | 96.2
| TSI | 0.0 | 3.0 | 97.0
| HapMapRevision=28
}}[[rs3794260]], a SNP in the [[KIAA0789]] gene, was associated with risk for [[hypertension]] in a study involving 1,500+ Japanese patients. The odds ratio associated with the risk allele, [[rs3794260(G)]], which is also the most common allele, is 1.26 (CI: 1.12 - 1.42, p = 0.0001). {{PMID|18003638}}

Note that another SNP in the [[KIAA0789]] gene, [[rs9739493]], was determined to be in a different linkage disequilibrium block, and is thus thought to be an independent risk factor for [[hypertension]]. {{PMID|18003638}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}