rs121913638, MYH7

N. diseases: 4
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, 1 (disorder)
163 0.851 0.120 14 23425980 missense variant C/T snv 0.800 1.000 22 1992 2005
Cardiomyopathy, Hypertrophic, Familial
355 0.851 0.120 14 23425980 missense variant C/T snv 0.700 1.000 13 1994 2017
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.120 14 23425980 missense variant C/T snv 0.700 1.000 12 1994 2017
Asymmetric Septal Hypertrophy
CUI: C0205700
Disease: Asymmetric Septal Hypertrophy
7 0.851 0.120 14 23425980 missense variant C/T snv 0.010 1.000 1 2009 2009