MYBPC3, myosin binding protein C3, 4607

N. diseases: 100; N. variants: 418
Disease: Congestive heart failure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs371401403
rs371401403
Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3
CUI: C0018802
Disease:
Congestive heart failure 		0.010 GeneticVariation BEFREE Homozygous missense MYBPC3 Pro873His mutation associated with increased risk for heart failure development in hypertrophic cardiomyopathy. 29663722 2018