rs863225119, 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, Familial Hypertrophic, 2
CUI: C1861864
Disease: Cardiomyopathy, Familial Hypertrophic, 2
30 0.882 0.080 1 201359632 missense variant T/A snv 0.800 1.000 1 2011 2011
CARDIOMYOPATHY, DILATED, 1D (disorder)
CUI: C1832243
Disease: CARDIOMYOPATHY, DILATED, 1D (disorder)
24 0.882 0.080 1 201359632 missense variant T/A snv 0.700 0
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
CUI: C2676271
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.882 0.080 1 201359632 missense variant T/A snv 0.700 0
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
96 0.882 0.080 1 201359632 missense variant T/A snv 0.010 1.000 1 2011 2011
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.882 0.080 1 201359632 missense variant T/A snv 0.010 1.000 1 2011 2011