TNNI3, troponin I3, cardiac type, 7137

N. diseases: 159; N. variants: 50
Disease: Restrictive cardiomyopathy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs727503503
rs727503503
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0007196
Disease:
Restrictive cardiomyopathy 		T 0.700 CausalMutation CLINVAR Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy. 20031618 2009
dbSNP: rs727503503
rs727503503
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0007196
Disease:
Restrictive cardiomyopathy 		T 0.700 CausalMutation CLINVAR Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype. 17599605 2007