{{Rsnum
|rsid=1941958
|Chromosome=18
|position=51200506
|Orientation=plus
|GMAF=0.4972
|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 | 25.7 | 44.2 | 30.1
| HCB | 40.4 | 47.8 | 11.8
| JPT | 36.6 | 51.8 | 11.6
| YRI | 20.5 | 50.7 | 28.8
| ASW | 26.8 | 41.1 | 32.1
| CHB | 40.4 | 47.8 | 11.8
| CHD | 27.5 | 59.6 | 12.8
| GIH | 29.7 | 49.5 | 20.8
| LWK | 18.2 | 51.8 | 30.0
| MEX | 41.4 | 41.4 | 17.2
| MKK | 25.0 | 55.1 | 19.9
| TSI | 20.8 | 49.5 | 29.7
| HapMapRevision=28
}}{{omim
|desc=HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 8; HYT8
|id=611014
|rsnum=1941958
}}

{{omim
|desc=HYPERTENSION, ESSENTIAL
|id=145500
|rsnum=1941958
}}

{{PMID Auto
|PMID=17015768
|Title=Implication of chromosome 18 in hypertension by sibling pair and association analyses: putative involvement of the RKHD2 gene.
}}

{{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}}