Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs6901221 0.925 0.160 6 33130499 downstream gene variant A/C snv 0.13 2
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 1
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 1
rs1857066
LOC100506023 ; TNFSF4
1.000 0.040 1 173363490 non coding transcript exon variant A/C snv 0.79 1
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 1
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 1
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 2
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 2
rs3130573
PSORS1C2 ; PSORS1C1
1.000 0.040 6 31138491 non coding transcript exon variant A/C;G snv 8.1E-06; 0.33 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs2516399 0.925 0.120 6 31513522 upstream gene variant A/G snv 0.11 3
rs3117230 0.882 0.200 6 33107858 upstream gene variant A/G snv 0.28 3
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 3
rs987870
HLA-DPA1 ; HLA-DPB1
0.851 0.160 6 33075103 intron variant A/G snv 0.19 3
rs443198
NOTCH4
0.851 0.200 6 32222629 synonymous variant A/G snv 0.38 0.39 2
rs10220668
LINC01500
1.000 0.040 14 59042487 intron variant A/G snv 0.30 1
rs1535001
ANKS1A
0.925 0.080 6 34959503 intron variant A/G snv 0.47 1
rs2359661
ITGAM
1.000 0.040 16 31269826 intron variant A/G snv 0.48 1
rs3093024
LOC105378122 ; CCR6
0.882 0.200 6 167119305 non coding transcript exon variant A/G snv 0.61 1
rs3792783
TNIP1
0.882 0.280 5 151076171 intron variant A/G snv 0.25 1