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: rs63750009
rs63750009
PSEN1
5 0.851 0.120 14 73192760 missense variant A/C;G snv 0.010 1.000 1 2010 2010
dbSNP: rs63750082
rs63750082
PSEN1
13 0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs63750083
rs63750083
PSEN1
13 0.732 0.160 14 73219177 missense variant C/A;T snv 0.010 1.000 1 2006 2006
dbSNP: rs63750110
rs63750110
PSEN2
1 1.000 0.080 1 226895548 missense variant A/C snv 3.6E-05 3.5E-05 0.010 1.000 1 2001 2001
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: 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: rs63750306
rs63750306
PSEN1
17 0.701 0.320 14 73173663 missense variant A/C;G;T snv 0.010 1.000 1 2016 2016
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: rs63750399
rs63750399
APP
3 0.882 0.080 21 25891787 missense variant T/A;C snv 0.010 1.000 1 1997 1997
dbSNP: rs63750424
rs63750424
MAPT
30 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2014 2014
dbSNP: rs63750487
rs63750487
PSEN1
3 0.882 0.120 14 73192771 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs63750524
rs63750524
PSEN1
2 1.000 0.080 14 73198095 missense variant A/C snv 0.010 1.000 1 2007 2007
dbSNP: rs63750569
rs63750569
PSEN1
2 0.925 0.080 14 73192711 missense variant G/A snv 0.010 1.000 1 2019 2019
dbSNP: rs63750588
rs63750588
PSEN1
3 0.925 0.080 14 73173687 missense variant T/A snv 0.010 1.000 1 2004 2004
dbSNP: rs63750599
rs63750599
PSEN1
7 0.827 0.160 14 73170963 missense variant T/C snv 0.010 1.000 1 2004 2004
dbSNP: rs63750646
rs63750646
PSEN1
6 0.807 0.120 14 73217147 missense variant G/C snv 0.010 1.000 1 1999 1999
dbSNP: rs63750666
rs63750666
PSEN2
2 0.925 0.080 1 226895521 missense variant C/T snv 3.6E-05 2.1E-05 0.010 1.000 1 2003 2003
dbSNP: rs63750687
rs63750687
PSEN1
33 0.752 0.200 14 73217137 missense variant C/A;G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs63750734
rs63750734
APP
4 0.851 0.080 21 25891790 missense variant C/T snv 0.010 1.000 1 1999 1999
dbSNP: rs63750756
rs63750756
MAPT
23 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 0.010 1.000 1 2010 2010
dbSNP: rs63750802
rs63750802
PSEN1
7 0.851 0.080 14 73219144 missense variant T/G snv 0.010 1.000 1 2007 2007
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: rs63750815
rs63750815
PSEN1
3 0.882 0.080 14 73170974 missense variant G/T snv 0.010 1.000 1 2002 2002
dbSNP: rs63750852
rs63750852
PSEN1
8 0.790 0.120 14 73170998 missense variant G/A;T snv 0.010 1.000 1 2008 2008
dbSNP: rs63750888
rs63750888
PSEN1
2 0.925 0.080 14 73192828 missense variant A/C snv 0.010 1.000 1 2006 2006