rs200411226, MYBPC3

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.
Familial Hypertrophic Cardiomyopathy Type 4
CUI: C1861862
Disease: Familial Hypertrophic Cardiomyopathy Type 4
145 0.851 0.080 11 47342718 missense variant C/T snv 2.4E-05 4.2E-05 0.800 1.000 3 1998 2011
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.080 11 47342718 missense variant C/T snv 2.4E-05 4.2E-05 0.700 1.000 22 1998 2017
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.851 0.080 11 47342718 missense variant C/T snv 2.4E-05 4.2E-05 0.700 1.000 13 1998 2013
LEFT VENTRICULAR NONCOMPACTION 10
CUI: C3715165
Disease: LEFT VENTRICULAR NONCOMPACTION 10
20 0.851 0.080 11 47342718 missense variant C/T snv 2.4E-05 4.2E-05 0.700 0