rs397516088, 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, Familial Hypertrophic, 1 (disorder)
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
163 0.882 0.080 14 23429850 missense variant C/G;T snv 0.700 1.000 20 1992 2005
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.882 0.080 14 23429850 missense variant C/G;T snv 0.700 1.000 9 2003 2019
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.882 0.080 14 23429850 missense variant C/G;T snv 0.700 1.000 4 2003 2017
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.882 0.080 14 23429850 missense variant C/G;T snv 0.700 0