{{Rsnum
|rsid=9739493
|Gene=WSCD2
|Chromosome=12
|position=108250412
|Orientation=plus
|GMAF=0.4421
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=WSCD2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 26.5 | 44.2 | 29.2
| HCB | 17.5 | 46.0 | 36.5
| JPT | 22.1 | 47.8 | 30.1
| YRI | 78.2 | 19.7 | 2.0
| ASW | 68.4 | 29.8 | 1.8
| CHB | 17.5 | 46.0 | 36.5
| CHD | 19.3 | 47.7 | 33.0
| GIH | 19.8 | 45.5 | 34.7
| LWK | 65.1 | 29.4 | 5.5
| MEX | 19.0 | 51.7 | 29.3
| MKK | 53.2 | 39.7 | 7.1
| TSI | 24.5 | 46.1 | 29.4
| HapMapRevision=28
}}[[rs9739493]], 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, [[rs9739493(T)]], was not directly reported. {{PMID|18003638}}

Note that another SNP in the [[KIAA0789]] gene, [[rs3794260]], 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 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}}