Disease: Immune System Diseases
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 4
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 4
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs6859219
ANKRD55
0.925 0.160 5 56142753 intron variant C/A snv 0.20 4
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5