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: 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 2013 2013
dbSNP: rs201085152
rs201085152
APP
3 0.925 0.080 21 25975072 missense variant G/A;T snv 1.6E-05; 3.6E-05 0.010 1.000 1 2008 2008
dbSNP: rs63750306
rs63750306
17 0.701 0.320 14 73173663 missense variant A/C;G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs63750424
rs63750424
30 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2008 2008
dbSNP: rs74315411
rs74315411
4 0.882 0.160 20 4699767 missense variant A/G snv 0.010 1.000 1 2014 2014