rs397515905, MYBPC3

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.
Familial Hypertrophic Cardiomyopathy Type 4
145 0.851 0.080 11 47342719 missense variant G/A;C;T snv 4.0E-06; 8.0E-06 0.700 1.000 20 1995 2017
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.080 11 47342719 missense variant G/A;C;T snv 4.0E-06; 8.0E-06 0.700 1.000 18 1998 2017
Cardiomyopathy, Hypertrophic, Familial
355 0.851 0.080 11 47342719 missense variant G/A;C;T snv 4.0E-06; 8.0E-06 0.700 1.000 15 1998 2017
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
163 0.851 0.080 11 47342719 missense variant G/A;C;T snv 4.0E-06; 8.0E-06 0.700 1.000 8 2008 2015
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.851 0.080 11 47342719 missense variant G/A;C;T snv 4.0E-06; 8.0E-06 0.700 0