Disease: Immune System Diseases
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
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 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
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
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 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
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3