Gene: APP ×
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 0.030 0.667 3 2014 2015
dbSNP: rs1223904774
rs1223904774
APP
8 0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs200620364
rs200620364
APP
2 0.925 0.080 21 26021849 missense variant C/T snv 0.010 1.000 1 2019 2019
dbSNP: rs63750734
rs63750734
APP
4 0.851 0.080 21 25891790 missense variant C/T snv 0.010 1.000 1 2019 2019
dbSNP: rs772069024
rs772069024
APP
3 0.882 0.080 21 26021858 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2019 2019