Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607129
rs267607129
TNNI3
0.800 GeneticVariation UNIPROT Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy. 21846512

2012
dbSNP: rs267607130
rs267607130
TNNI3
0.800 GeneticVariation UNIPROT Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy. 21846512

2012
dbSNP: rs267607129
rs267607129
TNNI3
0.800 GeneticVariation UNIPROT Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy. 19590045

2009
dbSNP: rs267607130
rs267607130
TNNI3
0.800 GeneticVariation UNIPROT Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy. 19590045

2009
dbSNP: rs267607129
rs267607129
TNNI3
C 0.800 CausalMutation CLINVAR

dbSNP: rs267607130
rs267607130
TNNI3
G 0.800 CausalMutation CLINVAR

dbSNP: rs397516354
rs397516354
TNNI3
T 0.700 GeneticVariation 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
dbSNP: rs777177571
rs777177571
TNNI3
0.700 GeneticVariation UNIPROT Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy. 21846512

2012
dbSNP: rs397516354
rs397516354
TNNI3
T 0.700 GeneticVariation CLINVAR Sarcomere protein gene mutations in patients with apical hypertrophic cardiomyopathy. 21511876

2011
dbSNP: rs777177571
rs777177571
TNNI3
0.700 GeneticVariation UNIPROT Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy. 19590045

2009
dbSNP: rs397516354
rs397516354
TNNI3
T 0.700 GeneticVariation CLINVAR Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences. 15698845

2005
dbSNP: rs397516354
rs397516354
TNNI3
T 0.700 GeneticVariation CLINVAR Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy. 15607392

2004
dbSNP: rs397516354
rs397516354
TNNI3
T 0.700 GeneticVariation CLINVAR Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy. 12860912

2003
dbSNP: rs397516349
rs397516349
TNNI3
T 0.700 CausalMutation CLINVAR

dbSNP: rs397516354
rs397516354
TNNI3
T 0.700 CausalMutation CLINVAR

dbSNP: rs727503504
rs727503504
TNNI3
C 0.700 GeneticVariation CLINVAR