Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1129
Gene Symbol: CHRM2
CHRM2
0.020 GeneticVariation disease BEFREE Previously, we reported a missense mutation (C722G) in the M2-muscarinic acetylcholine receptor (CHRM2) gene associated with familial dilated cardiomyopathy. 23743182 2013
Entrez Id: 1129
Gene Symbol: CHRM2
CHRM2
0.020 GeneticVariation disease BEFREE A missense mutation in the CHRM2 gene is associated with familial dilated cardiomyopathy. 18451336 2008