Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12713559
rs12713559
APOB
10 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.010 1.000 1 1995 1995
dbSNP: rs879254842
rs879254842
LDLR ; MIR6886
3 0.882 0.080 19 11113326 missense variant T/C snv 0.010 1.000 1 2006 2006