Gene: APP ×
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: rs63749964
rs63749964
APP
4 0.851 0.080 21 25891783 missense variant A/C snv 0.710 1.000 21 1991 2005
dbSNP: rs1200601649
rs1200601649
APP
2 0.925 0.080 21 26022022 missense variant A/C snv 0.010 1.000 1 2019 2019
dbSNP: rs201093867
rs201093867
APP
2 0.925 0.080 21 26021995 missense variant A/C snv 0.010 1.000 1 2019 2019
dbSNP: rs1315025573
rs1315025573
APP
2 0.925 0.080 21 25891849 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs113145702
rs113145702
APP
1 1.000 0.080 21 25955632 missense variant A/G snv 0.010 1.000 1 2019 2019
dbSNP: rs1191863771
rs1191863771
APP
3 0.925 0.080 21 25911833 missense variant A/G snv 4.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs466433
rs466433
APP
1 1.000 0.080 21 26171645 intron variant A/G snv 8.3E-02 0.010 1.000 1 2015 2015
dbSNP: rs63751122
rs63751122
APP
2 0.925 0.080 21 25891765 missense variant A/G snv 0.710 1.000 1 2019 2019
dbSNP: rs778758780
rs778758780
APP
1 1.000 0.080 21 25975137 missense variant A/G snv 8.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs2830077
rs2830077
APP
1 1.000 0.080 21 26130406 intron variant C/A snv 0.38 0.010 1.000 1 2017 2017
dbSNP: rs63750264
rs63750264
APP
17 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.900 1.000 58 1991 2019
dbSNP: rs371425292
rs371425292
APP
10 0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 0.080 1.000 8 1998 2018
dbSNP: rs202218688
rs202218688
APP
2 1.000 0.080 21 26000131 missense variant C/A;T snv 4.0E-06; 5.6E-05 0.010 1.000 1 2019 2019
dbSNP: rs1260168075
rs1260168075
APP
1 1.000 0.080 21 25975217 missense variant C/G snv 0.010 1.000 1 2004 2004
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: rs772020679
rs772020679
APP
1 1.000 0.080 21 26053285 missense variant C/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs781215285
rs781215285
APP
1 1.000 0.080 21 26051030 missense variant C/G snv 4.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs63750064
rs63750064
APP
2 0.925 0.080 21 25897605 missense variant C/G;T snv 0.720 1.000 21 1991 2019
dbSNP: rs63750151
rs63750151
APP
3 0.882 0.080 21 25891761 missense variant C/G;T snv 0.020 1.000 2 2006 2018
dbSNP: rs63750579
rs63750579
APP
13 0.742 0.280 21 25891856 missense variant C/G;T snv 0.020 1.000 2 2000 2002
dbSNP: rs772069024
rs772069024
APP
3 0.882 0.080 21 26021858 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs63750066
rs63750066
APP
9 0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 0.730 1.000 25 1991 2017
dbSNP: rs63750734
rs63750734
APP
4 0.851 0.080 21 25891790 missense variant C/T snv 0.730 1.000 23 1991 2019
dbSNP: rs63750847
rs63750847
APP
8 0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 0.100 0.818 11 2012 2018
dbSNP: rs63749810
rs63749810
APP
3 0.882 0.200 21 25891853 missense variant C/T snv 0.720 1.000 10 2001 2019