rs74315379, TNNT2

N. diseases: 6
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)
24 0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 0.800 1.000 17 2000 2017
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 0.720 1.000 13 2001 2016
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 0.700 1.000 12 2001 2013
Cardiomyopathy, Familial Hypertrophic, 2
30 0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 0.700 1.000 10 2001 2015
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 0.700 1.000 10 2001 2015
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 0.020 1.000 2 2003 2016