rs397515897, MYBPC3

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
355 0.882 0.080 11 47343019 splice donor variant A/G snv 0.700 1.000 3 2009 2017
Familial Hypertrophic Cardiomyopathy Type 4
145 0.882 0.080 11 47343019 splice donor variant A/G snv 0.700 0
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.882 0.080 11 47343019 splice donor variant A/G snv 0.700 0