rs397516484, 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
30 0.851 0.080 1 201359244 missense variant C/G;T snv 1.2E-05 0.800 1.000 19 1994 2014
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
163 0.851 0.080 1 201359244 missense variant C/G;T snv 1.2E-05 0.700 1.000 8 1997 2015
CARDIOMYOPATHY, DILATED, 1D (disorder)
24 0.851 0.080 1 201359244 missense variant C/G;T snv 1.2E-05 0.700 1.000 6 2003 2014
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.851 0.080 1 201359244 missense variant C/G;T snv 1.2E-05 0.700 1.000 6 2003 2014
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.851 0.080 1 201359244 missense variant C/G;T snv 1.2E-05 0.700 0