rs587782962, MYH7

N. diseases: 2
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.
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.925 0.080 14 23422267 missense variant C/T snv 6.4E-05 7.7E-05 0.710 1.000 3 2004 2017
Cardiomyopathy, Hypertrophic, Familial
355 0.925 0.080 14 23422267 missense variant C/T snv 6.4E-05 7.7E-05 0.700 1.000 7 2004 2017