Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099594 1.000 0.040 18 49464790 upstream gene variant A/C;G;T snv 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs11465802
IL23R ; C1orf141
1.000 0.040 1 67219915 intron variant A/C;T snv 1
rs1373692 1.000 0.040 5 40431081 non coding transcript exon variant A/C;T snv 1
rs9926095
NKD1
1.000 0.040 16 50645404 3 prime UTR variant A/C;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
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs3764147
LACC1
0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 3
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs3828309
ATG16L1
0.882 0.160 2 233271764 intron variant A/G snv 0.42 3
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 3
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 2
rs1250546
ZMIZ1
0.925 0.080 10 79272775 intron variant A/G snv 0.36 2
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 2
rs2076756
NOD2
0.882 0.040 16 50722970 intron variant A/G snv 0.17 2
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2