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: rs63750847
rs63750847
APP
8 0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 0.020 1.000 2 2014 2017
dbSNP: rs1699102
rs1699102
SORL1
3 0.882 0.080 11 121586253 missense variant C/G;T snv 3.2E-05; 0.53 0.010 1.000 1 2017 2017
dbSNP: rs405509
rs405509
APOE
30 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 0.010 1.000 1 2017 2017