Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
0.110 GeneticVariation disease LHGDN Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene. 16651346 2006
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
0.110 GeneticVariation disease CLINVAR A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy. 10525521 1999