Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 4
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 4
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 4
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 3
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 2
rs12924729
CLEC16A
0.882 0.200 16 11093926 intron variant G/A snv 0.34 2
rs2293370
TIMMDC1
0.882 0.160 3 119501087 intron variant G/A snv 0.18 2
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 2
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13 2
rs6974491
ELMO1
0.807 0.120 7 37334906 intron variant G/A snv 0.14 2
rs7208487
FBXL20
0.925 0.080 17 39387196 intron variant T/A;G snv 2
rs10931468
NAB1
0.925 0.080 2 190673836 intron variant C/A;G;T snv 1
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 1
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 1
rs1372072
PLCL2
0.851 0.200 3 16913767 intron variant G/A snv 0.35 1
rs3745516
SPIB
0.925 0.080 19 50423485 intron variant A/G snv 0.62 1
rs3790567
IL12RB2
0.851 0.240 1 67356694 intron variant A/G snv 0.61 1
rs4679904 0.925 0.080 3 160623108 intergenic variant C/G;T snv 1
rs485499
LINC01100 ; IL12A-AS1
0.925 0.080 3 160028076 intron variant T/C snv 0.29 1
rs4938534
BTG4 ; POU2AF1
0.925 0.080 11 111404408 intron variant G/A snv 0.56 1
rs538147
RPS6KA4
0.925 0.080 11 64362250 intron variant G/A snv 0.29 1