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: rs11136000
rs11136000
CLU
19 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.100 1.000 12 2010 2018
dbSNP: rs10524523
rs10524523
TOMM40
7 0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 0.080 0.875 8 2010 2017
dbSNP: rs6656401
rs6656401
CR1
8 0.776 0.200 1 207518704 intron variant A/G;T snv 0.070 1.000 7 2011 2018
dbSNP: rs3764650
rs3764650
ABCA7
9 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.030 1.000 3 2015 2020
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: rs4877365
rs4877365
DAPK1
4 0.851 0.120 9 87540777 intron variant G/A snv 0.28 0.030 1.000 3 2006 2012
dbSNP: rs4878104
rs4878104
DAPK1
4 0.851 0.120 9 87578076 intron variant C/T snv 0.40 0.030 1.000 3 2006 2012
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: rs11754661
rs11754661
MTHFD1L
6 0.851 0.120 6 150885942 intron variant G/A;T snv 0.020 1.000 2 2010 2012
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: rs17070145
rs17070145
WWC1
10 0.790 0.120 5 168418786 intron variant C/T snv 0.43 0.020 0.500 2 2011 2017
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: rs2075650
rs2075650
TOMM40
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.020 1.000 2 2013 2017
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: 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: rs10410544
rs10410544
SIRT2
6 0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 0.010 1.000 1 2014 2014
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: 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