CHRM3, cholinergic receptor muscarinic 3, 1131

N. diseases: 284; N. variants: 17
Disease: Epilepsy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12059546
rs12059546
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0014544
Disease:
Epilepsy 		G 0.800 GeneticVariation GWASCAT Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. 22949513 2012
dbSNP: rs12059546
rs12059546
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0014544
Disease:
Epilepsy 		G 0.800 GeneticVariation GWASDB Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. 22949513 2012