Source: CLINVAR

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C1861864
Disease: Cardiomyopathy, Familial Hypertrophic, 2
Cardiomyopathy, Familial Hypertrophic, 2 		disease 0.900 strong 1.000 91 26 1991 2019
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C1832243
Disease: CARDIOMYOPATHY, DILATED, 1D (disorder)
CARDIOMYOPATHY, DILATED, 1D (disorder) 		disease 0.900 strong 1.000 91 24 1991 2019
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		disease 0.800 definitive 0.982 86 19 1991 2018
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		group 0.700 None 1.000 0 3 2004 2019
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		group 0.630 None 1.000 37 13 2000 2019
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C2676271
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder) 		disease 0.600 strong 1.000 91 21 1991 2019
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		disease 0.500 None 1.000 6 7 1996 2006
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		disease 0.430 None 1.000 0 3 2001 2005
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		disease 0.110 None 1.000 1 1 1999 2006
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		disease 0.100 None 1.000 8 1 1997 2015
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		troponin T2, cardiac type 0.601 0.423 2.0E-03
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		disease 0.100 None 0 1