Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 4
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 2
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 2
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 2
rs1857066
LOC100506023 ; TNFSF4
1.000 0.040 1 173363490 non coding transcript exon variant A/C snv 0.79 1
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 1
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 1
rs3130573
PSORS1C2 ; PSORS1C1
1.000 0.040 6 31138491 non coding transcript exon variant A/C;G snv 8.1E-06; 0.33 1
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 4
rs1535001
ANKS1A
0.925 0.080 6 34959503 intron variant A/G snv 0.47 2
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 2
rs4554699 0.925 0.040 1 161638578 intergenic variant A/G snv 2
rs987870
HLA-DPA1 ; HLA-DPB1
0.851 0.160 6 33075103 intron variant A/G snv 0.19 2
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs2516399 0.925 0.120 6 31513522 upstream gene variant A/G snv 0.11 1
rs2834167
IL10RB
0.752 0.360 21 33268483 missense variant A/G snv 0.33 0.25 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
rs4134466
ATG5
1.000 0.040 6 106129493 intron variant A/G snv 0.70 1