Disease: Immune System Diseases
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 4
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 4
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 4
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 3
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 4
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs934734
SPRED2
0.925 0.160 2 65368452 intron variant G/A;T snv 0.54 4
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs212389
LOC105378083 ; LOC112267968
0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 3
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 4
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13