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: rs13397985
rs13397985
SP110 ; SP140
5 0.827 0.280 2 230226508 intron variant T/C;G snv 0.700 1.000 4 2008 2014
dbSNP: rs7176508
rs7176508
DRAIC
4 0.851 0.280 15 69726651 intron variant A/G snv 0.67 0.700 1.000 4 2008 2014
dbSNP: rs735665
rs735665
GRAMD1B
8 0.776 0.280 11 123490689 intron variant G/A snv 0.15 0.700 1.000 4 2008 2014
dbSNP: rs872071
rs872071
IRF4
13 0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 0.700 1.000 4 2008 2014
dbSNP: rs17483466
rs17483466
ACOXL ; MIR4435-2HG
5 0.827 0.280 2 111039881 intron variant A/G snv 0.15 0.700 1.000 3 2008 2013
dbSNP: rs9880772
rs9880772 		5 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 0.700 1.000 3 2016 2017
dbSNP: rs140522
rs140522
ODF3B
11 0.851 0.160 22 50532837 upstream gene variant T/A;C snv 0.700 1.000 2 2017 2019
dbSNP: rs1679013
rs1679013 		3 0.882 0.160 9 22206988 intron variant C/A;T snv 0.43 0.700 1.000 2 2013 2017
dbSNP: rs210142
rs210142
BAK1 ; GGNBP1
3 0.925 0.120 6 33579060 intron variant T/C snv 0.74 0.700 1.000 2 2012 2013
dbSNP: rs210143
rs210143
BAK1 ; GGNBP1
6 0.827 0.160 6 33579153 intron variant T/C snv 0.74 0.700 1.000 2 2017 2017
dbSNP: rs2511714
rs2511714 		2 0.925 0.120 8 102566646 regulatory region variant T/G snv 0.41 0.700 1.000 2 2013 2016
dbSNP: rs35923643
rs35923643
GRAMD1B
3 0.925 0.120 11 123484683 intron variant A/G snv 0.15 0.700 1.000 2 2016 2017
dbSNP: rs391855
rs391855 		2 0.925 0.120 16 85895015 upstream gene variant A/T snv 0.52 0.700 1.000 2 2016 2017
dbSNP: rs4368253
rs4368253 		2 0.925 0.120 18 59955055 TF binding site variant T/A;C snv 0.700 1.000 2 2013 2016
dbSNP: rs4406737
rs4406737
FAS
2 0.925 0.120 10 88999967 intron variant A/G snv 0.50 0.700 1.000 2 2013 2016
dbSNP: rs58055674
rs58055674
ACOXL ; MIR4435-2HG
2 0.925 0.120 2 111074216 intron variant T/C snv 0.13 0.700 1.000 2 2016 2017
dbSNP: rs8024033
rs8024033 		2 0.925 0.120 15 40111456 upstream gene variant C/G snv 0.50 0.700 1.000 2 2016 2017
dbSNP: rs10028805
rs10028805
BANK1
3 0.882 0.160 4 101816093 intron variant G/A snv 0.45 0.700 1.000 1 2016 2016
dbSNP: rs10069690
rs10069690
TERT
53 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs1036935
rs1036935 		2 0.925 0.120 18 50317164 upstream gene variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1044873
rs1044873
IRF8
2 0.925 0.120 16 85922065 3 prime UTR variant C/T snv 0.40 0.700 1.000 1 2014 2014
dbSNP: rs10936599
rs10936599
MYNN
32 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 0.700 1.000 1 2014 2014
dbSNP: rs11083846
rs11083846
PRKD2
3 0.882 0.200 19 46704397 splice region variant G/A snv 0.17 0.16 0.700 1.000 1 2008 2008
dbSNP: rs11636802
rs11636802
LOC105370831
2 0.925 0.120 15 56483399 intergenic variant A/G snv 8.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs11637565
rs11637565
DRAIC
2 0.925 0.120 15 69728186 intron variant G/A snv 0.66 0.700 1.000 1 2017 2017