rs727504246, 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 0.827 0.080 1 201363330 missense variant G/A snv 0.800 1.000 4 2000 2017
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.827 0.080 1 201363330 missense variant G/A snv 0.710 1.000 3 2000 2004
CARDIOMYOPATHY, DILATED, 1D (disorder)
24 0.827 0.080 1 201363330 missense variant G/A snv 0.700 1.000 4 2000 2017
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
21 0.827 0.080 1 201363330 missense variant G/A snv 0.700 1.000 4 2000 2017
Cardiomyopathy, Hypertrophic, Familial
355 0.827 0.080 1 201363330 missense variant G/A snv 0.010 1.000 1 2000 2000