{{Rsnum
|rsid=12638540
|Gene=CMTM7
|Chromosome=3
|position=32447042
|Orientation=plus
|GMAF=0.04545
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CMTM7
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 92.9 | 6.2 | 0.9
| HCB | 79.6 | 19.0 | 1.5
| JPT | 92.9 | 7.1 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 79.6 | 19.0 | 1.5
| CHD | 90.8 | 8.3 | 0.9
| GIH | 90.1 | 9.9 | 0.0
| LWK | 91.8 | 8.2 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 87.7 | 11.6 | 0.6
| TSI | 92.2 | 7.8 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20400778
|Trait=Mortality among heart failure patients
|Title=Genomic Variation Associated with Mortality among Adults of European and African Ancestry with Heart Failure: The CHARGE Consortium
|RiskAllele=G
|Pval=3E-7
|OR=1.53
|ORtxt=[1.01-2.31]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}