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: rs10159239
rs10159239
NLRP3
3 0.882 0.040 1 247443750 intron variant G/A snv 0.57 0.010 1.000 1 2020 2020
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2019 2019
dbSNP: rs10767664
rs10767664
BDNF
16 0.752 0.400 11 27704439 intron variant T/A snv 0.83 0.010 1.000 1 2014 2014
dbSNP: rs10811656
rs10811656
CDKN2B-AS1
7 0.807 0.200 9 22124473 intron variant C/T snv 0.47 0.010 1.000 1 2016 2016
dbSNP: rs10846744
rs10846744
SCARB1
11 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.010 1.000 1 2018 2018
dbSNP: rs10918859
rs10918859
NOS1AP
3 0.882 0.040 1 162199478 intron variant G/A snv 0.16 0.010 1.000 1 2013 2013
dbSNP: rs11014166
rs11014166
CACNB2
10 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.010 1.000 1 2010 2010
dbSNP: rs11057830
rs11057830
SCARB1
5 0.851 0.040 12 124822507 intron variant G/A snv 0.15 0.010 1.000 1 2019 2019
dbSNP: rs1122608
rs1122608
SMARCA4
16 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.010 1.000 1 2016 2016
dbSNP: rs11234027
rs11234027
NADSYN1
5 0.882 0.080 11 71523061 intron variant G/A snv 0.24 0.010 1.000 1 2015 2015
dbSNP: rs12040273
rs12040273
GALNT2
3 0.882 0.040 1 230063651 intron variant C/T snv 0.28 0.010 1.000 1 2018 2018
dbSNP: rs12050217
rs12050217
BDKRB1
6 0.827 0.160 14 96262416 intron variant A/G snv 0.21 0.010 1.000 1 2014 2014
dbSNP: rs12115090
rs12115090
CRISPLD1
3 0.882 0.040 8 75012585 intron variant A/C snv 0.33 0.44 0.010 1.000 1 2018 2018
dbSNP: rs12344245
rs12344245
FAM189A2
3 0.882 0.040 9 69340801 intron variant A/G snv 0.12 0.010 1.000 1 2018 2018
dbSNP: rs12704673
rs12704673
CALCR
3 0.882 0.040 7 93525009 intron variant A/G;T snv 0.27 0.010 1.000 1 2019 2019
dbSNP: rs12785878
rs12785878
NADSYN1
25 0.677 0.520 11 71456403 intron variant G/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs12979860
rs12979860
IFNL4
84 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2015 2015
dbSNP: rs13306221
rs13306221
BDNF
4 0.851 0.120 11 27701142 intron variant C/T snv 5.9E-02 0.010 1.000 1 2014 2014
dbSNP: rs138760780
rs138760780
CDK18
3 0.882 0.040 1 205515245 intron variant C/T snv 1.5E-02 0.010 1.000 1 2018 2018
dbSNP: rs1408888
rs1408888
DACH1
5 0.851 0.120 13 71854515 intron variant T/G snv 0.30 0.010 1.000 1 2014 2014
dbSNP: rs1466535
rs1466535
LRP1
9 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs1467568
rs1467568
SIRT1
8 0.776 0.320 10 67915401 intron variant A/G snv 0.46 0.010 1.000 1 2017 2017
dbSNP: rs16941382
rs16941382
GOSR2 ; LRRC37A2
3 0.882 0.040 17 46966142 intron variant T/C snv 0.15 0.010 1.000 1 2017 2017
dbSNP: rs17251221
rs17251221
CASR
18 0.724 0.360 3 122274400 intron variant A/G snv 0.11 0.010 1.000 1 2013 2013
dbSNP: rs17293632
rs17293632
SMAD3
12 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.010 1.000 1 2016 2016