rs397516470, 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, DILATED, 1D (disorder)
24 0.851 0.080 1 201363377 inframe deletion CTC/- delins 0.700 1.000 9 1995 2016
Cardiomyopathy, Familial Hypertrophic, 2
30 0.851 0.080 1 201363377 inframe deletion CTC/- delins 0.700 1.000 9 1995 2016
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.851 0.080 1 201363377 inframe deletion CTC/- delins 0.700 1.000 9 1995 2016
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.080 1 201363377 inframe deletion CTC/- delins 0.700 1.000 8 1995 2012