TNNI3, troponin I3, cardiac type, 7137

N. diseases: 159; N. variants: 50
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894724
rs104894724
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1861861
Disease:
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
A 0.810 CausalMutation CLINVAR
dbSNP: rs104894729
rs104894729
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1861861
Disease:
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
T 0.810 CausalMutation CLINVAR
dbSNP: rs104894730
rs104894730
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1861861
Disease:
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
C 0.810 CausalMutation CLINVAR
dbSNP: rs121917760
rs121917760
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1861861
Disease:
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
T 0.810 CausalMutation CLINVAR
dbSNP: rs104894724
rs104894724
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1860752
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
C 0.800 CausalMutation CLINVAR
dbSNP: rs104894725
rs104894725
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1860752
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
G 0.800 CausalMutation CLINVAR
dbSNP: rs104894727
rs104894727
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1860752
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
T 0.800 CausalMutation CLINVAR
dbSNP: rs267607129
rs267607129
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C2750091
Disease:
Cardiomyopathy, Dilated, 1FF
C 0.800 CausalMutation CLINVAR
dbSNP: rs267607130
rs267607130
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C2750091
Disease:
Cardiomyopathy, Dilated, 1FF
G 0.800 CausalMutation CLINVAR
dbSNP: rs397516353
rs397516353
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1860752
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
A 0.800 CausalMutation CLINVAR
dbSNP: rs397516354
rs397516354
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1860752
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
T 0.800 CausalMutation CLINVAR
dbSNP: rs727504242
rs727504242
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1860752
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
A 0.800 GeneticVariation CLINVAR
dbSNP: rs104894729
rs104894729
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0007194
Disease:
Hypertrophic Cardiomyopathy
A 0.710 GeneticVariation CLINVAR
dbSNP: rs104894727
rs104894727
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0878544
Disease:
Cardiomyopathies
T 0.700 GeneticVariation CLINVAR
dbSNP: rs104894728
rs104894728
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1860752
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
C 0.700 CausalMutation CLINVAR
dbSNP: rs104894728
rs104894728
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1861861
Disease:
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
C 0.700 CausalMutation CLINVAR
dbSNP: rs104894729
rs104894729
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0949658
Disease:
Cardiomyopathy, Hypertrophic, Familial
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1114167340
rs1114167340
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1861861
Disease:
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
A 0.700 GeneticVariation CLINVAR
dbSNP: rs121917760
rs121917760
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0007194
Disease:
Hypertrophic Cardiomyopathy
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1349668884
rs1349668884
Entrez Id: 7137;352909;101930593
Gene Symbol: TNNI3;DNAAF3;LOC101930593
TNNI3;DNAAF3;LOC101930593
CUI: C1847554
Disease:
CILIARY DYSKINESIA, PRIMARY, 2 (disorder)
CT 0.700 CausalMutation CLINVAR
dbSNP: rs1349668884
rs1349668884
Entrez Id: 7137;352909;101930593
Gene Symbol: TNNI3;DNAAF3;LOC101930593
TNNI3;DNAAF3;LOC101930593
CUI: C0008780
Disease:
Ciliary Motility Disorders
CT 0.700 CausalMutation CLINVAR
dbSNP: rs267607127
rs267607127
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1860752
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
T 0.700 CausalMutation CLINVAR
dbSNP: rs267607128
rs267607128
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1860752
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
A 0.700 CausalMutation CLINVAR
dbSNP: rs368861241
rs368861241
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C1860752
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
A 0.700 CausalMutation CLINVAR
dbSNP: rs397516340
rs397516340
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0007194
Disease:
Hypertrophic Cardiomyopathy
A 0.700 GeneticVariation CLINVAR