Disease: Cardiomyopathy, Hypertrophic, Familial ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs368972037
rs368972037
Entrez Id: 5554;11272;100533464
Gene Symbol: PRH1;PRR4;PRH1-PRR4
PRH1;PRR4;PRH1-PRR4
CUI: C0949658
Disease:
Cardiomyopathy, Hypertrophic, Familial 		0.010 GeneticVariation BEFREE Exome sequencing identifies a novel MYH7 p.G407C mutation responsible for familial hypertrophic cardiomyopathy. 24963656 2014