Disease: Immune System Diseases
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
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
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 4
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 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
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
rs212389
LOC105378083 ; LOC112267968
0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 3
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 4
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5