Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3 		0.800 GeneticVariation disease CLINVAR High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians. 22876777 2012
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3 		0.800 GeneticVariation disease CLINVAR Sarcomere protein gene mutations in patients with apical hypertrophic cardiomyopathy. 21511876 2011
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3 		0.800 GeneticVariation disease CLINVAR Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences. 15698845 2005
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3 		0.800 GeneticVariation disease CLINVAR Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy. 15607392 2004
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3 		0.800 GeneticVariation disease CLINVAR Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy. 12860912 2003
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3 		0.800 CausalMutation disease CLINVAR
Entrez Id: 1410
Gene Symbol: CRYAB
CRYAB 		0.110 CausalMutation disease CLINVAR