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
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
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs7775759 0.925 0.200 6 31384669 upstream gene variant G/A snv 0.36 6
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs6933050 0.925 0.200 6 31375855 non coding transcript exon variant T/C snv 0.22 5
rs9266409 0.925 0.200 6 31368791 intron variant T/C snv 0.22 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs2253907 0.882 0.360 6 31369093 intron variant C/T snv 0.43 3
rs4947296 0.851 0.440 6 31090401 intergenic variant T/A;C snv 3
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 3
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 3
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 3
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 2
rs3757247
BACH2
0.827 0.320 6 90247744 intron variant C/T snv 0.38 2
rs7616215
CCR3 ; LOC105377067
0.925 0.280 3 46164194 intron variant C/T snv 0.62 2
rs2838519
GATD3A
0.851 0.280 21 44195140 intron variant G/A;C snv 2
rs9268861
HLA-DRB9
0.925 0.280 6 32462117 intron variant C/A snv 0.22 2
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 2