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: rs281865161
rs281865161
APP
2 0.925 0.080 21 25897626 missense variant TC/GA mnv 0.700 0
dbSNP: rs63749964
rs63749964
APP
4 0.851 0.080 21 25891783 missense variant A/C snv 0.700 0
dbSNP: rs63750066
rs63750066
APP
9 0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 0.700 0
dbSNP: rs63750264
rs63750264
APP
17 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.700 0
dbSNP: rs63750399
rs63750399
APP
3 0.882 0.080 21 25891787 missense variant T/A;C snv 0.700 0
dbSNP: rs63750643
rs63750643
APP
3 0.882 0.080 21 25891793 missense variant T/C snv 0.700 0
dbSNP: rs63750671
rs63750671
APP
8 0.790 0.240 21 25891858 missense variant G/C snv 0.700 0
dbSNP: rs63750734
rs63750734
APP
4 0.851 0.080 21 25891790 missense variant C/T snv 0.700 0
dbSNP: rs63750973
rs63750973
APP
3 0.882 0.120 21 25891792 missense variant G/A snv 0.700 0
dbSNP: rs63751039
rs63751039
APP
8 0.776 0.200 21 25891855 missense variant T/C snv 0.700 0