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: rs2244012
rs2244012
RAD50
1 1.000 0.080 5 132565533 intron variant A/G snv 0.33 0.820 1.000 1 2010 2016
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: rs3859192
rs3859192
GSDMA
3 0.925 0.080 17 39972395 intron variant C/T snv 0.42 0.820 1.000 1 2010 2016
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: rs7212938
rs7212938
GSDMA
1 0.925 0.120 17 39966427 missense variant G/A;C;T snv 4.1E-04; 4.2E-06; 0.52 0.820 0.750 1 2011 2015
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: rs10197862
rs10197862
IL18R1 ; IL1RL1
2 0.925 0.120 2 102350089 intron variant A/G snv 0.18 0.810 1.000 1 2011 2014
dbSNP: rs2786098
rs2786098
CRB1
1 1.000 0.080 1 197356778 intron variant T/A;G snv 0.810 1.000 1 2010 2010
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: rs404860
rs404860
NOTCH4
2 0.925 0.160 6 32216568 non coding transcript exon variant T/C snv 0.21 0.810 1.000 1 2011 2011
dbSNP: rs7130588
rs7130588 		3 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 0.810 1.000 1 2011 2011
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: rs9268516
rs9268516 		3 0.882 0.200 6 32411712 upstream gene variant C/T snv 0.24 0.810 1.000 1 2012 2012
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: rs987870
rs987870
HLA-DPA1 ; HLA-DPB1
3 0.851 0.160 6 33075103 intron variant A/G snv 0.19 0.810 1.000 1 2011 2011
dbSNP: rs992969
rs992969 		2 0.882 0.080 9 6209697 intergenic variant A/G;T snv 0.810 1.000 1 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: rs10508372
rs10508372 		1 1.000 0.080 10 8930055 intergenic variant G/A snv 0.14 0.800 1.000 1 2011 2011
dbSNP: rs1101999
rs1101999
PYHIN1
1 1.000 0.080 1 158962765 intron variant C/T snv 0.92 0.800 1.000 1 2011 2011
dbSNP: rs11214966
rs11214966
LOC101928940
1 1.000 0.080 11 114360533 intron variant T/C snv 0.13 0.800 1.000 1 2011 2011
dbSNP: rs1701704
rs1701704
IKZF4 ; LOC105369781
5 0.851 0.200 12 56018703 intron variant T/G snv 0.25 0.800 1.000 1 2011 2011
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: rs204993
rs204993
PBX2
3 0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 0.800 1.000 1 2011 2011
dbSNP: rs2069408
rs2069408
CDK2 ; PMEL
2 0.925 0.200 12 55970537 intron variant A/G snv 0.24 0.800 1.000 1 2011 2011
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