rs727504273, 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, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.925 0.080 14 23431781 missense variant T/G snv 7.0E-06 0.700 1.000 7 2003 2017
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
163 0.925 0.080 14 23431781 missense variant T/G snv 7.0E-06 0.700 0
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.925 0.080 14 23431781 missense variant T/G snv 7.0E-06 0.010 1.000 1 2005 2005