Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs10156091
ICA1
1.000 0.080 7 8147464 intron variant T/C snv 0.86 1
rs9271055
HLA-DRB1
1.000 0.080 6 32607592 intergenic variant G/T snv 0.84 1
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 2
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 3
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 1
rs389883
CYP21A2 ; STK19
0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 4
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs630379
NELFE ; CYP21A2
0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs638893 0.882 0.080 11 118827828 intergenic variant G/A snv 0.79 1
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs849141
JAZF1
0.851 0.240 7 28145472 intron variant A/G snv 0.78 1
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs659445
EHMT2 ; CYP21A2 ; C2
0.882 0.160 6 31896527 intron variant G/A;C snv 0.77 0.76 3
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 1
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 1
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 1
rs1518111
IL19 ; IL10
0.790 0.360 1 206771300 intron variant T/C snv 0.71 1
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 1