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: rs63750066
rs63750066
APP
9 0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 0.700 1.000 10 1992 2018
dbSNP: rs63750264
rs63750264
APP
17 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.080 1.000 8 1996 2019
dbSNP: rs63751019
rs63751019
PSEN1
3 0.925 0.080 14 73198066 missense variant C/G snv 0.020 1.000 2 1996 2004
dbSNP: rs429358
rs429358
APOE
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 8 1997 2016
dbSNP: rs63750215
rs63750215
PSEN2
19 0.701 0.240 1 226885603 missense variant A/T snv 0.050 1.000 5 1997 2010
dbSNP: rs63750231
rs63750231
PSEN1
23 0.689 0.160 14 73198100 missense variant A/C;G snv 0.050 1.000 5 1997 2016
dbSNP: rs765670175
rs765670175
PSEN1
7 0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 0.030 1.000 3 1997 2008
dbSNP: rs63749891
rs63749891
PSEN1
5 0.851 0.080 14 73198094 missense variant G/C;T snv 0.010 1.000 1 1997 1997
dbSNP: rs63750248
rs63750248
PSEN1
2 0.925 0.080 14 73198047 missense variant G/A;C;T snv 4.0E-06; 2.4E-05 0.010 1.000 1 1997 1997
dbSNP: rs63750399
rs63750399
APP
3 0.882 0.080 21 25891787 missense variant T/A;C snv 0.010 1.000 1 1997 1997
dbSNP: rs63751037
rs63751037
PSEN1
7 0.790 0.080 14 73173642 missense variant A/G snv 0.020 1.000 2 1998 2003
dbSNP: rs121917808
rs121917808
PSEN1
3 0.882 0.080 14 73219192 missense variant C/A snv 0.010 1.000 1 1998 1998
dbSNP: rs63750812
rs63750812
PSEN2
2 0.925 0.080 1 226885623 missense variant G/A snv 1.6E-05 1.4E-05 0.010 1.000 1 1998 1998
dbSNP: rs63750963
rs63750963
PSEN1
2 0.925 0.080 14 73186884 missense variant T/C snv 0.010 1.000 1 1998 1998
dbSNP: rs63751210
rs63751210
PSEN1
5 0.882 0.080 14 73186878 missense variant C/T snv 0.010 1.000 1 1998 1998
dbSNP: rs747363386
rs747363386
PSEN1
1 1.000 0.080 14 73173669 missense variant A/C;G snv 8.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs63749925
rs63749925
PSEN1
3 0.882 0.080 14 73219191 missense variant C/T snv 0.010 1.000 1 1999 1999
dbSNP: rs63750322
rs63750322
PSEN1
2 0.925 0.080 14 73173654 missense variant A/G;T snv 0.010 1.000 1 1999 1999
dbSNP: rs63750646
rs63750646
PSEN1
6 0.807 0.120 14 73217147 missense variant G/C snv 0.010 1.000 1 1999 1999
dbSNP: rs63750734
rs63750734
APP
4 0.851 0.080 21 25891790 missense variant C/T snv 0.010 1.000 1 1999 1999
dbSNP: rs63751416
rs63751416
PSEN1
2 0.925 0.080 14 73217170 missense variant C/G snv 0.010 1.000 1 1999 1999
dbSNP: rs17125721
rs17125721
PSEN1
14 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 0.040 0.500 4 2000 2013
dbSNP: rs1275544322
rs1275544322
APP
3 0.882 0.160 21 25975185 missense variant T/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs63750265
rs63750265
PSEN1
3 0.882 0.080 14 73186869 missense variant T/A;C;G snv 0.010 1.000 1 2000 2000
dbSNP: rs63751254
rs63751254
PSEN1
4 0.851 0.160 14 73217210 missense variant A/G snv 0.010 1.000 1 2000 2000