CHRM3, cholinergic receptor muscarinic 3, 1131

N. diseases: 284; N. variants: 17
Disease: Juvenile Myoclonic 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: C0270853
Disease:
Juvenile Myoclonic Epilepsy 		0.010 GeneticVariation BEFREE The search for syndrome-related susceptibility alleles identified significant associations for GAEs at 2q22.3 (rs10496964, P(meta) = 9.1 × 10(-9), OR[T] = 0.68) and at 1q43 for JME (rs12059546, P(meta) = 4.1 × 10(-8), OR[G] = 1.42). 22949513 2012