Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs574503121 1.000 0.120 6 33090337 downstream gene variant -/ATTT delins 4.3E-04 1
rs373094430 1.000 0.120 6 32622847 TF binding site variant -/C ins 1
rs201386475
HLA-DQB1
1.000 0.120 6 32668286 5 prime UTR variant -/CA delins 1
rs112630268
LINC00452
1.000 0.120 13 113919624 non coding transcript exon variant -/G ins 1
rs397897657
ICOSLG
1.000 0.120 21 44230126 intron variant -/G delins 1.7E-04 1
rs56323213
ICOSLG
1.000 0.120 21 44230126 intron variant -/G delins 1
rs113652681 1.000 0.120 6 33339623 downstream gene variant -/G;TG ins 1
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs2647046 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 3
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 3
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 3
rs2076538
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32349694 non coding transcript exon variant A/C snv 0.42 0.33 2
rs2524095
LINC02571 ; HLA-B ; LOC112267902
0.925 0.160 6 31298340 intron variant A/C snv 0.65 2
rs2858884 0.925 0.200 6 32732306 upstream gene variant A/C snv 0.23 2
rs3129878
HLA-DRA
0.807 0.360 6 32440958 intron variant A/C snv 0.30 2
rs518374
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32297933 intron variant A/C snv 0.33 2
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 2
rs9268862
HLA-DRB9
0.925 0.160 6 32462390 intron variant A/C snv 0.29 2
rs9269081
HLA-DRB9
0.851 0.280 6 32473323 intron variant A/C snv 0.69 2
rs1042127
CDSN ; PSORS1C1
0.925 0.120 6 31116393 missense variant A/C snv 0.21 0.17 1
rs11121380
SPSB1
1.000 0.120 1 9348900 intron variant A/C snv 0.11 1
rs12110787
MAP3K4
1.000 0.120 6 161053934 intron variant A/C snv 0.16 1
rs1480383 1.000 0.120 6 32773079 intergenic variant A/C snv 0.31 1
rs16906916
PCDH15
1.000 0.120 10 55089225 intron variant A/C snv 3.9E-02 1