rs397516457, TNNT2

N. diseases: 4
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, Familial Hypertrophic, 2
30 0.851 0.080 1 201365291 missense variant C/A;T snv 0.800 1.000 20 1991 2017
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.080 1 201365291 missense variant C/A;T snv 0.710 1.000 12 1999 2017
CARDIOMYOPATHY, DILATED, 1D (disorder)
24 0.851 0.080 1 201365291 missense variant C/A;T snv 0.700 1.000 8 1991 2017
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.851 0.080 1 201365291 missense variant C/A;T snv 0.700 1.000 8 1991 2017