rs74315380, TNNT2

N. diseases: 2
Source: BEFREE ×
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
CUI: C0007193
Disease: Cardiomyopathy, Dilated
65 0.851 0.080 1 201364366 missense variant G/A;C snv 0.720 1.000 2 2003 2016
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
200 0.851 0.080 1 201364366 missense variant G/A;C snv 0.020 1.000 2 2003 2016