Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121964856
rs121964856
TNNT2
0.800 GeneticVariation UNIPROT Sudden death due to troponin T mutations. 9060892

1997
dbSNP: rs121964856
rs121964856
TNNT2
T 0.800 CausalMutation CLINVAR Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy. 7898523

1995
dbSNP: rs121964856
rs121964856
TNNT2
0.800 GeneticVariation UNIPROT Clinical utility gene card for: hypertrophic cardiomyopathy (type 1-14). 21267010

2011
dbSNP: rs121964856
rs121964856
TNNT2
T 0.800 CausalMutation CLINVAR Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy. 10449439

1999
dbSNP: rs121964856
rs121964856
TNNT2
0.800 GeneticVariation UNIPROT A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy. 10525521

1999
dbSNP: rs121964856
rs121964856
TNNT2
0.800 GeneticVariation UNIPROT Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy. 9140840

1997
dbSNP: rs121964856
rs121964856
TNNT2
T 0.800 CausalMutation CLINVAR Shared genetic causes of cardiac hypertrophy in children and adults. 18403758

2008
dbSNP: rs121964856
rs121964856
TNNT2
T 0.800 CausalMutation CLINVAR Clinical manifestations of hypertrophic cardiomyopathy with mutations in the cardiac beta-myosin heavy chain gene or cardiac troponin T gene. 8951566

1996