rs28934573, TP53

N. diseases: 28
Disease: Familial dilated cardiomyopathy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial dilated cardiomyopathy
CUI: C0340427
Disease: Familial dilated cardiomyopathy
0.010 GeneticVariation BEFREE Previously, we reported a missense mutation (C722G) in the M2-muscarinic acetylcholine receptor (CHRM2) gene associated with familial dilated cardiomyopathy. 23743182 2013