rs727503513, TNNT2

N. diseases: 2
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.
Restrictive cardiomyopathy
CUI: C0007196
Disease: Restrictive cardiomyopathy
30 0.925 0.080 1 201365292 missense variant G/A snv 0.700 1.000 1 1999 1999
Cardiomyopathy, Familial Hypertrophic, 2
30 0.925 0.080 1 201365292 missense variant G/A snv 0.700 0