rs45586240, TNNT2

N. diseases: 7
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 0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 0.700 1.000 3 2009 2017
Cardiomyopathy, Familial Hypertrophic, 2
30 0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 0.700 1.000 3 2009 2017
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 0.700 1.000 3 2009 2017
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 0.700 0
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 0.700 0
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2009 2009
Hypertrophic obstructive cardiomyopathy
90 0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2009 2009