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
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
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
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 4
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 4
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 4