rs121964858, TNNT2

N. diseases: 6
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 0.807 0.120 1 201365244 missense variant A/C;G;T snv 0.800 1.000 14 1994 2012
CARDIOMYOPATHY, DILATED, 1D (disorder)
24 0.807 0.120 1 201365244 missense variant A/C;G;T snv 0.700 0
Cardiomyopathy, Hypertrophic, Familial
355 0.807 0.120 1 201365244 missense variant A/C;G;T snv 0.010 1.000 1 2000 2000
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.807 0.120 1 201365244 missense variant A/C;G;T snv 0.010 1.000 1 1998 1998
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.807 0.120 1 201365244 missense variant A/C;G;T snv 0.010 1.000 1 1998 1998
Hypertrophic obstructive cardiomyopathy
90 0.807 0.120 1 201365244 missense variant A/C;G;T snv 0.010 1.000 1 1998 1998