rs121964856, TNNT2

N. diseases: 8
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 201365297 missense variant C/A;T snv 0.800 1.000 29 1994 2015
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.807 0.120 1 201365297 missense variant C/A;T snv 0.730 1.000 18 1994 2020
CARDIOMYOPATHY, DILATED, 1D (disorder)
24 0.807 0.120 1 201365297 missense variant C/A;T snv 0.700 1.000 18 1994 2015
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.807 0.120 1 201365297 missense variant C/A;T snv 0.700 1.000 18 1994 2015
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.807 0.120 1 201365297 missense variant C/A;T snv 0.010 1.000 1 2016 2016
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.807 0.120 1 201365297 missense variant C/A;T snv 0.010 1.000 1 1999 1999
Hypertrophic obstructive cardiomyopathy
90 0.807 0.120 1 201365297 missense variant C/A;T snv 0.010 1.000 1 1997 1997
Mitochondrial pathology
CUI: C3825201
Disease: Mitochondrial pathology
6 0.807 0.120 1 201365297 missense variant C/A;T snv 0.010 1.000 1 1999 1999