rs148808089, 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, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.882 0.080 14 23429038 missense variant G/A snv 2.0E-05 1.4E-05 0.700 1.000 7 2006 2017
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
163 0.882 0.080 14 23429038 missense variant G/A snv 2.0E-05 1.4E-05 0.700 1.000 4 2006 2014
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.882 0.080 14 23429038 missense variant G/A snv 2.0E-05 1.4E-05 0.700 0
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.882 0.080 14 23429038 missense variant G/A snv 2.0E-05 1.4E-05 0.700 0