rs727503503, TNNI3

N. diseases: 5
Disease: Restrictive cardiomyopathy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Restrictive cardiomyopathy
CUI: C0007196
Disease: Restrictive cardiomyopathy
0.700 CausalMutation CLINVAR Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy. 20031618 2009
Restrictive cardiomyopathy
CUI: C0007196
Disease: Restrictive cardiomyopathy
0.700 CausalMutation CLINVAR Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype. 17599605 2007