rs36211715, 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, Familial Hypertrophic, 1 (disorder)
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
163 0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 0.800 1.000 39 1992 2017
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 0.720 1.000 16 1995 2017
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 16 1995 2017
Chest Pain
CUI: C0008031
Disease: Chest Pain
7 0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 0.700 0
Hypertrophic obstructive cardiomyopathy
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
90 0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2011 2011