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: rs10498633
rs10498633
SLC24A4
2 0.925 0.080 14 92460608 intron variant G/T snv 0.19 0.800 1.000 4 2013 2019
dbSNP: rs405697
rs405697
TOMM40
1 1.000 0.080 19 44901434 3 prime UTR variant A/G;T snv 0.800 1.000 4 2011 2019
dbSNP: rs7254776
rs7254776
LOC107985305
1 1.000 0.080 19 44724478 intron variant T/C;G snv 0.800 1.000 4 2009 2018
dbSNP: rs8103315
rs8103315
BCL3
2 1.000 0.080 19 44750911 intron variant C/A snv 9.1E-02 0.800 1.000 4 2011 2018
dbSNP: rs10948363
rs10948363
CD2AP
1 1.000 0.080 6 47520026 intron variant A/G snv 0.23 0.800 1.000 3 2013 2019
dbSNP: rs11610206
rs11610206
LOC105369746
2 0.925 0.080 12 47245743 intron variant T/C snv 9.7E-02 0.800 1.000 3 2009 2011
dbSNP: rs17643262
rs17643262
MARK4 ; PPP1R37
1 1.000 0.080 19 45128558 intron variant G/A snv 9.9E-02 0.800 1.000 3 2011 2018
dbSNP: rs35349669
rs35349669
INPP5D
2 0.925 0.080 2 233159830 intron variant C/T snv 0.35 0.800 1.000 3 2013 2019
dbSNP: rs7225151
rs7225151
SCIMP ; LOC100130950
1 1.000 0.080 17 5233752 intron variant G/A snv 0.15 0.800 1.000 3 2013 2019
dbSNP: rs983392
rs983392 		1 1.000 0.080 11 60156035 downstream gene variant A/G snv 0.28 0.800 1.000 3 2013 2019
dbSNP: rs10405693
rs10405693 		1 1.000 0.080 19 44823407 downstream gene variant C/T snv 0.28 0.800 1.000 2 2014 2019
dbSNP: rs1160985
rs1160985
TOMM40
6 1.000 0.080 19 44900155 intron variant C/T snv 0.52 0.800 1.000 2 2013 2019
dbSNP: rs11669338
rs11669338
NECTIN2
1 1.000 0.080 19 44879727 intron variant T/G snv 8.9E-02 0.800 1.000 2 2009 2018
dbSNP: rs12978931
rs12978931
NECTIN2
1 1.000 0.080 19 44860443 intron variant A/G snv 0.19 0.800 1.000 2 2011 2018
dbSNP: rs1562990
rs1562990
MS4A4A
2 0.925 0.080 11 60255614 intron variant C/A;T snv 0.800 1.000 2 2011 2011
dbSNP: rs1582763
rs1582763
MS4A4A
2 1.000 0.080 11 60254475 intron variant G/A snv 0.28 0.800 1.000 2 2011 2016
dbSNP: rs346763
rs346763
MARK4 ; EXOC3L2
1 1.000 0.080 19 45226017 intron variant G/A snv 0.10 0.800 1.000 2 2014 2018
dbSNP: rs471470
rs471470 		1 1.000 0.080 11 86120499 intergenic variant C/A;G snv 0.800 1.000 2 2011 2016
dbSNP: rs4803750
rs4803750
BCL3
22 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 0.800 1.000 2 2011 2019
dbSNP: rs4803760
rs4803760 		1 1.000 0.080 19 44830577 intergenic variant T/A;C snv 0.800 1.000 2 2011 2018
dbSNP: rs4939338
rs4939338 		1 1.000 0.080 11 60331752 upstream gene variant T/C snv 0.63 0.800 1.000 2 2011 2018
dbSNP: rs7114401
rs7114401 		1 1.000 0.080 11 86128893 intergenic variant C/T snv 0.66 0.800 1.000 2 2011 2018
dbSNP: rs7259620
rs7259620
APOE
2 0.925 0.120 19 44904531 upstream gene variant G/A;C snv 0.800 1.000 2 2013 2019
dbSNP: rs7274581
rs7274581
CASS4
1 1.000 0.080 20 56443204 intron variant T/C snv 0.12 0.800 1.000 2 2013 2019
dbSNP: rs760136
rs760136
TOMM40
1 1.000 0.080 19 44900601 intron variant A/G snv 0.52 0.800 1.000 2 2013 2018