{{Rsnum
|rsid=12059546
|Gene=CHRM3
|Chromosome=1
|position=239806797
|Orientation=plus
|GMAF=0.3205
|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 | 60.2 | 33.6 | 6.2
| HCB | 57.7 | 37.2 | 5.1
| JPT | 42.5 | 43.4 | 14.2
| YRI | 12.9 | 51.0 | 36.1
| ASW | 24.6 | 45.6 | 29.8
| CHB | 57.7 | 37.2 | 5.1
| CHD | 44.0 | 49.5 | 6.4
| GIH | 65.3 | 32.7 | 2.0
| LWK | 13.8 | 49.5 | 36.7
| MEX | 74.1 | 22.4 | 3.4
| MKK | 19.2 | 46.8 | 34.0
| TSI | 66.7 | 30.4 | 2.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22949513
  |Trait=Epilepsy (generalized)
  |Title=Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
  |RiskAllele=G
  |Pval=4E-8
  |OR=1.42
  |ORtxt=[1.26-1.61]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}