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: rs63750512
rs63750512
MAPT
6 0.827 0.160 17 46024010 missense variant G/A;C snv 1.2E-05 0.020 1.000 2 1999 2000
dbSNP: rs63750129
rs63750129
MAPT
4 0.882 0.120 17 45996612 missense variant A/C snv 4.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs63750570
rs63750570
MAPT
8 0.827 0.120 17 46018629 missense variant G/A snv 0.010 1.000 1 2001 2001
dbSNP: rs63750635
rs63750635
MAPT
5 0.851 0.120 17 46014286 missense variant C/T snv 0.010 1.000 1 2002 2002
dbSNP: rs760073870
rs760073870
CAPN2
1 1 223752954 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 0.010 1.000 1 2002 2002
dbSNP: rs1189501362
rs1189501362
GSK3B
4 0.882 0.120 3 119863583 missense variant G/A snv 7.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs1205185774
rs1205185774
AHSA1
4 0.882 0.120 14 77469161 missense variant C/T snv 0.010 1.000 1 2003 2003
dbSNP: rs1235948930
rs1235948930
MAPT
4 0.882 0.120 17 45983865 missense variant C/T snv 7.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs63750349
rs63750349
MAPT
5 0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs63750376
rs63750376
MAPT
7 0.827 0.120 17 45996657 missense variant G/T snv 0.010 < 0.001 1 2003 2003
dbSNP: rs866604606
rs866604606
MAPK1
4 0.882 0.120 22 21772907 missense variant G/A snv 0.010 1.000 1 2003 2003
dbSNP: rs63750756
rs63750756
MAPT
23 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 0.030 1.000 3 1999 2007
dbSNP: rs1005752506
rs1005752506
AMPH
1 7 38461398 missense variant G/A snv 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs1300858963
rs1300858963
OGA
1 10 101799033 missense variant G/A snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs281860580
rs281860580
HLA-B ; HLA-C
1 6 31270083 missense variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs376388064
rs376388064
VEGFA
1 6 43782006 missense variant C/T snv 2.8E-05 3.5E-05 0.010 1.000 1 2017 2017
dbSNP: rs63750416
rs63750416
MAPT
7 0.851 0.120 17 46010373 missense variant A/C snv 0.010 1.000 1 2017 2017
dbSNP: rs763872192
rs763872192
CD36
4 0.882 0.080 7 80672000 missense variant C/T snv 2.8E-05 0.010 1.000 1 2017 2017
dbSNP: rs769483065
rs769483065
HSP90AA1
1 14 102085426 missense variant G/A;T snv 8.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs775645890
rs775645890
UPK3B
1 7 76515192 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs779612015
rs779612015
UPK3B
1 7 76515186 missense variant C/T snv 4.7E-06 0.010 1.000 1 2017 2017
dbSNP: rs63750424
rs63750424
MAPT
30 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.070 1.000 7 2002 2018
dbSNP: rs201792381
rs201792381
APP
2 1.000 0.080 21 25997384 missense variant G/A;C snv 1.6E-05 0.020 1.000 2 2018 2018
dbSNP: rs587778556
rs587778556
NFE2L2
2 2 177231705 missense variant G/A snv 3.2E-05 4.9E-05 0.020 1.000 2 2014 2018
dbSNP: rs755135182
rs755135182
NFE2L2
2 2 177231657 missense variant G/A snv 4.0E-06 0.020 1.000 2 2014 2018