Disease: Immune System Diseases
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
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
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
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
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 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
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs13314993
LOC105377022
0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5