Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 6
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs2305479
GSDMB
0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 4
rs7219923
GSDMB
0.882 0.160 17 39918265 non coding transcript exon variant C/T snv 0.52 4
rs9303281
GSDMB
0.882 0.160 17 39917793 non coding transcript exon variant G/A snv 0.50 4
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 4
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 3
rs9901146 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 3
rs3859192
GSDMA
0.925 0.080 17 39972395 intron variant C/T snv 0.42 3
rs4795400
GSDMB
0.925 0.080 17 39910767 intron variant C/T snv 0.36 3
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 3
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs907092
IKZF3
0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36 3
rs12603332
LOC112268187 ; ORMDL3 ; LRRC3C
0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 3
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 3
rs4795405
LRRC3C
0.851 0.160 17 39932164 intron variant T/A;C snv 3
rs8076131
ORMDL3
0.790 0.200 17 39924659 intron variant G/A;C snv 3