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
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 2
rs3818753
JAK1
1.000 0.200 1 64873549 3 prime UTR variant A/G snv 1.0E-02 3.6E-03 2
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 1
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 1
rs1518111
IL19 ; IL10
0.790 0.360 1 206771300 intron variant T/C snv 0.71 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 1
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs924080 0.882 0.240 1 67294457 intergenic variant T/C snv 0.45 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs17006292
TFCP2L1
1.000 0.200 2 121261187 intron variant C/A snv 2.8E-02 1
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 1
rs7572482
STAT4
1.000 0.200 2 191150346 intron variant A/C;G snv 1
rs7574070
STAT4
1.000 0.200 2 191145762 intron variant A/C snv 0.55 1
rs897200
STAT4
0.851 0.280 2 191153045 upstream gene variant T/C snv 0.54 1
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs7616215
CCR3 ; LOC105377067
0.925 0.280 3 46164194 intron variant C/T snv 0.62 2
rs1874886
IL12A-AS1
0.925 0.280 3 160011868 non coding transcript exon variant G/A snv 0.41 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 2
rs936551
CPLX1
1.000 0.200 4 827702 upstream gene variant A/G snv 0.52 1
rs10050860
ERAP1
0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16 1