rs104894724
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
A
0.810
CausalMutation
CLINVAR
rs104894729
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
T
0.810
CausalMutation
CLINVAR
rs104894730
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
C
0.810
CausalMutation
CLINVAR
rs121917760
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
T
0.810
CausalMutation
CLINVAR
rs104894728
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
C
0.700
CausalMutation
CLINVAR
rs1114167340
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
A
0.700
GeneticVariation
CLINVAR
rs397516349
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
T
0.700
CausalMutation
CLINVAR
rs397516354
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
T
0.700
GeneticVariation
CLINVAR
Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.
15607392
2004
rs397516354
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
T
0.700
GeneticVariation
CLINVAR
Sarcomere protein gene mutations in patients with apical hypertrophic cardiomyopathy.
21511876
2011
rs397516354
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
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
rs397516354
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
T
0.700
CausalMutation
CLINVAR
rs397516354
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
T
0.700
GeneticVariation
CLINVAR
Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.
15698845
2005
rs397516354
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
T
0.700
GeneticVariation
CLINVAR
Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy.
12860912
2003
rs727503504
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
C
0.700
GeneticVariation
CLINVAR