rs397516463, 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
CUI: C1861864
Disease: Cardiomyopathy, Familial Hypertrophic, 2
30 0.851 0.080 1 201364369 missense variant G/A snv 1.4E-05 0.800 1.000 19 1994 2014
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.080 1 201364369 missense variant G/A snv 1.4E-05 0.700 1.000 12 1996 2017
CARDIOMYOPATHY, DILATED, 1D (disorder)
CUI: C1832243
Disease: CARDIOMYOPATHY, DILATED, 1D (disorder)
24 0.851 0.080 1 201364369 missense variant G/A snv 1.4E-05 0.700 1.000 7 2003 2014
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
CUI: C2676271
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.851 0.080 1 201364369 missense variant G/A snv 1.4E-05 0.700 1.000 7 2003 2014