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: rs573658040
rs573658040
APOE
9 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.010 1.000 1 2006 2006
dbSNP: rs769455
rs769455
APOE
8 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 0.010 1.000 1 2006 2006