Source: GWASDB ×
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: rs1342326
rs1342326 		2 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 0.840 1.000 3 2010 2020
dbSNP: rs10192157
rs10192157
IL18R1 ; IL1RL1
2 1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 0.710 1.000 1 2010 2020
dbSNP: rs3117098
rs3117098
HCG23 ; TSBP1-AS1
4 0.851 0.280 6 32390736 non coding transcript exon variant G/A snv 0.72 0.810 1.000 1 2011 2020
dbSNP: rs3939286
rs3939286 		2 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 0.710 1.000 1 2010 2020
dbSNP: rs7775228
rs7775228 		5 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 0.810 0.500 1 2011 2020
dbSNP: rs11071559
rs11071559
RORA
1 0.925 0.080 15 60777789 intron variant C/T snv 0.23 0.820 1.000 3 2010 2019
dbSNP: rs1837253
rs1837253 		2 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 0.840 0.929 3 2010 2019
dbSNP: rs907092
rs907092
IKZF3
3 0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36 0.810 1.000 3 2010 2019
dbSNP: rs1008723
rs1008723
GSDMB
3 0.925 0.160 17 39910014 intron variant G/C;T snv 0.800 1.000 1 2011 2019
dbSNP: rs12936231
rs12936231
ZPBP2
3 0.925 0.160 17 39872867 intron variant C/G;T snv 0.720 1.000 1 2011 2019
dbSNP: rs17843604
rs17843604
HLA-DQA1
2 0.925 0.120 6 32652506 intergenic variant C/T snv 0.49 0.800 1.000 1 2010 2019
dbSNP: rs3771180
rs3771180
IL18R1 ; IL1RL1
2 1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 0.820 1.000 1 2011 2019
dbSNP: rs9272346
rs9272346
HLA-DQA1
6 0.790 0.320 6 32636595 intron variant G/A snv 0.54 0.810 1.000 1 2012 2019
dbSNP: rs928413
rs928413
IL33
2 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 0.800 1.000 1 2010 2019
dbSNP: rs9901146
rs9901146 		3 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 0.800 1.000 1 2011 2019
dbSNP: rs992969
rs992969 		2 0.882 0.080 9 6209697 intergenic variant A/G;T snv 0.810 1.000 1 2010 2019
dbSNP: rs2305480
rs2305480
GSDMB
7 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 0.860 0.900 4 2008 2018
dbSNP: rs7216389
rs7216389
GSDMB
3 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.900 0.889 4 2007 2018
dbSNP: rs1295686
rs1295686
IL13 ; TH2LCRR
2 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 0.840 1.000 3 2010 2018
dbSNP: rs11078927
rs11078927
GSDMB
2 0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 0.820 1.000 2 2011 2018
dbSNP: rs2305479
rs2305479
GSDMB
4 0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 0.800 1.000 1 2011 2018
dbSNP: rs3763309
rs3763309
BTNL2 ; TSBP1-AS1
3 0.882 0.160 6 32408196 upstream gene variant C/A;T snv 0.800 1.000 1 2011 2018
dbSNP: rs4129267
rs4129267
IL6R
5 0.807 0.200 1 154453788 intron variant C/G;T snv 0.820 0.667 1 2011 2018
dbSNP: rs7927894
rs7927894 		5 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 0.820 0.750 1 2011 2018
dbSNP: rs8069176
rs8069176 		3 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 0.740 1.000 1 2008 2018