{{Rsnum
|rsid=536477
|Gene=CHRM3
|Chromosome=1
|position=239882608
|Orientation=plus
|GMAF=0.4757
|Gene_s=CHRM3
|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 | 18.6 | 49.6 | 31.9
| HCB | 14.6 | 39.4 | 46.0
| JPT | 8.8 | 51.3 | 39.8
| YRI | 61.9 | 34.0 | 4.1
| ASW | 57.1 | 41.1 | 1.8
| CHB | 14.6 | 39.4 | 46.0
| CHD | 10.1 | 53.2 | 36.7
| GIH | 21.8 | 49.5 | 28.7
| LWK | 62.7 | 33.6 | 3.6
| MEX | 17.2 | 56.9 | 25.9
| MKK | 48.1 | 39.7 | 12.2
| TSI | 20.6 | 42.2 | 37.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=
  |Pval=3E-9
  |OR=1.59
  |ORtxt=[NR]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}