TNNT2, troponin T2, cardiac type, 7139

N. diseases: 79; N. variants: 73
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121964857
rs121964857
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1861864
Disease:
Cardiomyopathy, Familial Hypertrophic, 2
A 0.800 CausalMutation CLINVAR
dbSNP: rs121964858
rs121964858
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1861864
Disease:
Cardiomyopathy, Familial Hypertrophic, 2
T 0.800 CausalMutation CLINVAR
dbSNP: rs121964860
rs121964860
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1832243
Disease:
CARDIOMYOPATHY, DILATED, 1D (disorder)
A 0.800 CausalMutation CLINVAR
dbSNP: rs727504246
rs727504246
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1861864
Disease:
Cardiomyopathy, Familial Hypertrophic, 2
0.800 GeneticVariation UNIPROT
dbSNP: rs863225119
rs863225119
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1861864
Disease:
Cardiomyopathy, Familial Hypertrophic, 2
A 0.800 GeneticVariation CLINVAR
dbSNP: rs121964857
rs121964857
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0007194
Disease:
Hypertrophic Cardiomyopathy
A 0.710 GeneticVariation CLINVAR
dbSNP: rs727504245
rs727504245
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0949658
Disease:
Cardiomyopathy, Hypertrophic, Familial
A 0.710 GeneticVariation CLINVAR
dbSNP: rs111344408
rs111344408
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0340427
Disease:
Familial dilated cardiomyopathy
G 0.700 GeneticVariation CLINVAR
dbSNP: rs111377893
rs111377893
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1861864
Disease:
Cardiomyopathy, Familial Hypertrophic, 2
G 0.700 GeneticVariation CLINVAR
dbSNP: rs121964857
rs121964857
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0949658
Disease:
Cardiomyopathy, Hypertrophic, Familial
A 0.700 CausalMutation CLINVAR
dbSNP: rs121964857
rs121964857
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0949658
Disease:
Cardiomyopathy, Hypertrophic, Familial
A 0.700 GeneticVariation CLINVAR
dbSNP: rs121964858
rs121964858
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1832243
Disease:
CARDIOMYOPATHY, DILATED, 1D (disorder)
T 0.700 CausalMutation CLINVAR
dbSNP: rs121964861
rs121964861
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1832243
Disease:
CARDIOMYOPATHY, DILATED, 1D (disorder)
T 0.700 CausalMutation CLINVAR
dbSNP: rs1289914935
rs1289914935
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0043202
Disease:
Wolff-Parkinson-White Syndrome
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558225569
rs1558225569
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1861864
Disease:
Cardiomyopathy, Familial Hypertrophic, 2
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558225569
rs1558225569
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C2676271
Disease:
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558225569
rs1558225569
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1832243
Disease:
CARDIOMYOPATHY, DILATED, 1D (disorder)
T 0.700 GeneticVariation CLINVAR
dbSNP: rs397516454
rs397516454
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0007193
Disease:
Cardiomyopathy, Dilated
C 0.700 GeneticVariation CLINVAR
dbSNP: rs397516461
rs397516461
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0007193
Disease:
Cardiomyopathy, Dilated
T 0.700 GeneticVariation CLINVAR
dbSNP: rs397516465
rs397516465
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0340427
Disease:
Familial dilated cardiomyopathy
A 0.700 GeneticVariation CLINVAR
dbSNP: rs397516482
rs397516482
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0949658
Disease:
Cardiomyopathy, Hypertrophic, Familial
A 0.700 GeneticVariation CLINVAR
dbSNP: rs397516484
rs397516484
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0878544
Disease:
Cardiomyopathies
G 0.700 CausalMutation CLINVAR
dbSNP: rs45466197
rs45466197
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C1861864
Disease:
Cardiomyopathy, Familial Hypertrophic, 2
0.700 GeneticVariation UNIPROT
dbSNP: rs45586240
rs45586240
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0878544
Disease:
Cardiomyopathies
A 0.700 GeneticVariation CLINVAR
dbSNP: rs45586240
rs45586240
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0007193
Disease:
Cardiomyopathy, Dilated
A 0.700 GeneticVariation CLINVAR