rs121913632, MYH7

N. diseases: 3
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 0.882 0.080 14 23425760 missense variant C/A;G;T snv 0.800 1.000 33 1992 2017
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.882 0.080 14 23425760 missense variant C/A;G;T snv 0.700 1.000 22 1993 2017
Cardiomyopathy, Hypertrophic, Familial
355 0.882 0.080 14 23425760 missense variant C/A;G;T snv 0.700 1.000 19 1985 2017