{{Rsnum
|rsid=1805762
|Gene=M6PR
|Chromosome=12
|position=8945306
|Orientation=minus
|GMAF=0.09963
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=M6PR
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 0.0 | 1.6 | 98.4
| HCB | 6.7 | 28.9 | 64.4
| JPT | 11.4 | 40.9 | 47.7
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 6.7 | 28.9 | 64.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}[[rs1805762]], a SNP in the [[M6PR]] gene, was associated with risk for [[hypertension]] in a study involving 1,500+ Japanese patients. The odds ratio associated with the risk allele, in dbSNP orientation, [[rs1805762(G)]], which is also the most common allele, is 1.23 (CI: 1.10 - 1.37, p = 0.0003). {{PMID|18003638}}

A SNP in close linkage, [[rs1805740]], has also been reported in association with [[hypertension]] risk in the large 2007 study reported by the Wellcome Trust Consortium. {{PMID|17554300|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}