Disease: Immune System Diseases
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs13314993
LOC105377022
0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5
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
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs6859219
ANKRD55
0.925 0.160 5 56142753 intron variant C/A snv 0.20 4
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7