Disease: Immune System Diseases
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
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
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 4
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 4
rs4750316
LINC02649 ; LINC02656
0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 4
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs6859219
ANKRD55
0.925 0.160 5 56142753 intron variant C/A snv 0.20 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 4
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 4
rs934734
SPRED2
0.925 0.160 2 65368452 intron variant G/A;T snv 0.54 4
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 4
rs212389
LOC105378083 ; LOC112267968
0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 3
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 3