rs121964860, TNNT2

N. diseases: 3
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 0.882 0.080 1 201361988 missense variant C/A;G;T snv 0.800 1.000 9 2000 2017
Cardiomyopathy, Familial Hypertrophic, 2
CUI: C1861864
Disease: Cardiomyopathy, Familial Hypertrophic, 2
30 0.882 0.080 1 201361988 missense variant C/A;G;T snv 0.700 1.000 1 2015 2015
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
CUI: C2676271
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.882 0.080 1 201361988 missense variant C/A;G;T snv 0.700 1.000 1 2015 2015