rs74315380, TNNT2

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
CARDIOMYOPATHY, DILATED, 1D (disorder)
CUI: C1832243
Disease: CARDIOMYOPATHY, DILATED, 1D (disorder)
24 0.851 0.080 1 201364366 missense variant G/A;C snv 0.800 1.000 14 2000 2017
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.851 0.080 1 201364366 missense variant G/A;C snv 0.720 1.000 8 2003 2016
Cardiomyopathy, Familial Hypertrophic, 2
CUI: C1861864
Disease: Cardiomyopathy, Familial Hypertrophic, 2
30 0.851 0.080 1 201364366 missense variant G/A;C snv 0.700 1.000 7 2004 2013
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
CUI: C2676271
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.851 0.080 1 201364366 missense variant G/A;C snv 0.700 1.000 7 2004 2013
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.851 0.080 1 201364366 missense variant G/A;C snv 0.020 1.000 2 2003 2016