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: rs610932
rs610932
MS4A6A
5 0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 0.040 1.000 4 2015 2018
dbSNP: rs3818361
rs3818361
CR1
6 0.851 0.080 1 207611623 intron variant A/G snv 0.74 0.030 1.000 3 2010 2014
dbSNP: rs5984894
rs5984894
PCDH11X
2 0.925 0.080 X 92138738 intron variant A/G snv 0.54 0.030 1.000 3 2009 2010
dbSNP: rs10997477
rs10997477
CTNNA3 ; LRRTM3 ; LOC101928961
1 1.000 0.080 10 67000961 intron variant C/T snv 0.31 0.020 1.000 2 2012 2014
dbSNP: rs11622883
rs11622883 		1 1.000 0.080 14 94689439 regulatory region variant T/A snv 0.37 0.020 1.000 2 2011 2017
dbSNP: rs137875858
rs137875858
UNC5C
2 0.925 0.080 4 95170280 missense variant G/A snv 2.9E-04 2.6E-04 0.020 1.000 2 2014 2016
dbSNP: rs145999145
rs145999145
PLD3
2 0.925 0.080 19 40371688 missense variant G/A snv 3.1E-03 3.6E-03 0.020 1.000 2 2018 2019
dbSNP: rs165932
rs165932
PSEN1
2 0.925 0.080 14 73198145 intron variant G/A;T snv 0.61 0.020 1.000 2 2006 2008
dbSNP: rs16923760
rs16923760
CTNNA3 ; LOC101928961
1 1.000 0.080 10 66920370 intron variant T/C snv 0.12 0.020 1.000 2 2012 2014
dbSNP: rs1784933
rs1784933
SORL1
3 0.882 0.080 11 121618707 intron variant G/A snv 0.84 0.020 1.000 2 2015 2017
dbSNP: rs1925608
rs1925608
CTNNA3 ; LRRTM3 ; LOC101928961
1 1.000 0.080 10 66990654 intron variant A/C snv 0.49 0.020 0.500 2 2012 2014
dbSNP: rs1925609
rs1925609
CTNNA3 ; LRRTM3 ; LOC101928961
1 1.000 0.080 10 66995149 intron variant T/C snv 0.51 0.020 1.000 2 2012 2014
dbSNP: rs2070045
rs2070045
SORL1
4 0.851 0.080 11 121577381 synonymous variant T/G snv 0.32 0.23 0.020 1.000 2 2014 2015
dbSNP: rs498055
rs498055 		2 0.925 0.080 10 95595157 non coding transcript exon variant C/A;G;T snv 0.39 0.020 0.500 2 2006 2008
dbSNP: rs597668
rs597668
MARK4 ; BLOC1S3
3 0.925 0.080 19 45205630 intron variant T/A;C;G snv 0.020 0.500 2 2011 2012
dbSNP: rs689021
rs689021
SORL1
2 0.925 0.080 11 121500411 intron variant G/A snv 0.40 0.020 0.500 2 2015 2017
dbSNP: rs9331949
rs9331949
CLU ; EPHX2
2 0.925 0.080 8 27597169 3 prime UTR variant T/C snv 6.2E-02 4.7E-02 0.020 1.000 2 2013 2017
dbSNP: rs1012381950
rs1012381950
POLB
1 1.000 0.080 8 42353758 intron variant T/C snv 0.010 1.000 1 2019 2019
dbSNP: rs10197851
rs10197851
HPCAL1
1 1.000 0.080 2 10345283 intron variant A/G snv 0.52 0.010 1.000 1 2011 2011
dbSNP: rs10410711
rs10410711
ZNF566
1 1.000 0.080 19 36449796 synonymous variant A/G snv 3.3E-02 3.5E-02 0.010 1.000 1 2015 2015
dbSNP: rs10421862
rs10421862
ZNF566
1 1.000 0.080 19 36474174 intron variant G/T snv 0.10 0.010 1.000 1 2015 2015
dbSNP: rs10498633
rs10498633
SLC24A4
2 0.925 0.080 14 92460608 intron variant G/T snv 0.19 0.010 1.000 1 2016 2016
dbSNP: rs1059507
rs1059507
LPL
4 1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 0.010 1.000 1 2017 2017
dbSNP: rs1060743
rs1060743
BIN1
2 0.925 0.080 2 127068957 synonymous variant A/G snv 0.34 0.29 0.010 1.000 1 2014 2014
dbSNP: rs10824310
rs10824310
PRKG1 ; PRKG1-AS1
1 1.000 0.080 10 52268704 intron variant C/T snv 4.7E-02 0.010 1.000 1 2017 2017