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: rs63750579
rs63750579
APP
13 0.742 0.280 21 25891856 missense variant C/G;T snv 0.800 1.000 6 1990 2010
dbSNP: rs63749810
rs63749810
APP
3 0.882 0.200 21 25891853 missense variant C/T snv 0.800 0
dbSNP: rs63750671
rs63750671
APP
8 0.790 0.240 21 25891858 missense variant G/C snv 0.700 0
dbSNP: rs63750921
rs63750921
APP
4 0.882 0.200 21 25891820 missense variant G/C snv 0.700 0
dbSNP: rs63751039
rs63751039
APP
8 0.776 0.200 21 25891855 missense variant T/C snv 0.700 0