Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 1
rs7574070
STAT4
1.000 0.200 2 191145762 intron variant A/C snv 0.55 1
rs6910516 1.000 0.200 6 31376050 non coding transcript exon variant A/C;G snv 1
rs7572482
STAT4
1.000 0.200 2 191150346 intron variant A/C;G snv 1
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs3818753
JAK1
1.000 0.200 1 64873549 3 prime UTR variant A/G snv 1.0E-02 3.6E-03 2
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 2
rs12212193
BACH2
0.925 0.280 6 90287050 intron variant A/G snv 0.38 1
rs13210247
TRAF3IP2-AS1 ; TRAF3IP2
0.882 0.280 6 111601517 non coding transcript exon variant A/G snv 0.10 1
rs1522596 1.000 0.200 7 150538695 downstream gene variant A/G snv 0.47 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs1916012 1.000 0.200 7 150536739 intergenic variant A/G snv 0.49 1
rs4795067
NOS2
0.882 0.280 17 27779649 intron variant A/G snv 0.31 1
rs7028891
DELEC1
0.925 0.280 9 114882735 intron variant A/G snv 0.50 1
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27 1
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs9266490 1.000 0.200 6 31372381 intron variant A/G snv 0.22 1
rs936551
CPLX1
1.000 0.200 4 827702 upstream gene variant A/G snv 0.52 1
rs9268861
HLA-DRB9
0.925 0.280 6 32462117 intron variant C/A snv 0.22 2
rs17006292
TFCP2L1
1.000 0.200 2 121261187 intron variant C/A snv 2.8E-02 1