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: rs63750264
rs63750264
APP
17 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.020 1.000 2 1997 2000
dbSNP: rs63750311
rs63750311
8 0.790 0.240 14 73192647 missense variant A/C snv 0.020 1.000 2 2000 2002
dbSNP: rs63750424
rs63750424
30 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.020 1.000 2 2000 2015
dbSNP: rs781049584
rs781049584
APP
18 0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 0.020 1.000 2 2009 2014
dbSNP: rs1035071612
rs1035071612
9 0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs10908821
rs10908821
1 1.000 0.040 1 161038745 intron variant C/G snv 0.11 0.010 1.000 1 2012 2012
dbSNP: rs1412095491
rs1412095491
APP
3 0.882 0.200 21 26051053 missense variant C/G snv 4.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs191838178
rs191838178
2 0.925 0.160 22 40407449 missense variant C/T snv 2.4E-05 7.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs2774276
rs2774276
1 1.000 0.040 1 161041926 intron variant G/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs2794521
rs2794521
CRP
15 0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 0.010 1.000 1 2011 2011
dbSNP: rs3091244
rs3091244
CRP
17 0.724 0.280 1 159714875 upstream gene variant G/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs3093075
rs3093075
5 0.882 0.120 1 159710123 upstream gene variant G/T snv 0.13 0.010 1.000 1 2011 2011
dbSNP: rs34487851
rs34487851
3 0.882 0.200 2 106026098 regulatory region variant A/G snv 0.28 0.010 1.000 1 2018 2018
dbSNP: rs63750215
rs63750215
19 0.701 0.240 1 226885603 missense variant A/T snv 0.010 1.000 1 2000 2000
dbSNP: rs63750522
rs63750522
8 0.827 0.120 14 73173644 missense variant G/A;C snv 0.010 1.000 1 2000 2000
dbSNP: rs63750579
rs63750579
APP
13 0.742 0.280 21 25891856 missense variant C/G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs63750671
rs63750671
APP
8 0.790 0.240 21 25891858 missense variant G/C snv 0.010 1.000 1 1998 1998
dbSNP: rs6910730
rs6910730
3 0.925 0.080 6 41278895 intron variant A/G snv 0.21 0.010 1.000 1 2015 2015
dbSNP: rs74315409
rs74315409
13 0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05 0.010 1.000 1 2003 2003
dbSNP: rs765670175
rs765670175
7 0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs79524815
rs79524815
4 0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 0.010 1.000 1 2018 2018