rs1566535410, MYH7

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, DILATED, 1S
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
53 0.851 0.080 14 23429297 missense variant T/C snv 0.700 0
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
163 0.851 0.080 14 23429297 missense variant T/C snv 0.700 0
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.080 14 23429297 missense variant T/C snv 0.700 0
Left ventricular noncompaction
CUI: C1960469
Disease: Left ventricular noncompaction
26 0.851 0.080 14 23429297 missense variant T/C snv 0.700 0
Mitral Valve Insufficiency
CUI: C0026266
Disease: Mitral Valve Insufficiency
11 0.851 0.080 14 23429297 missense variant T/C snv 0.700 0