Source: ALL
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 59
rs113993959
CFTR
0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 25
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 9
rs1800693
TNFRSF1A
0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 9
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13 7
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs6974491
ELMO1
0.807 0.120 7 37334906 intron variant G/A snv 0.14 6
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 6
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 5
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 5
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 4
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 4
rs7208487
FBXL20
0.925 0.080 17 39387196 intron variant T/A;G snv 4
rs3790567
IL12RB2
0.851 0.240 1 67356694 intron variant A/G snv 0.61 4
rs1372072
PLCL2
0.851 0.200 3 16913767 intron variant G/A snv 0.35 4
rs911263
RAD51B
0.851 0.200 14 68286876 intron variant C/T snv 0.57 4
rs12924729
CLEC16A
0.882 0.200 16 11093926 intron variant G/A snv 0.34 3
rs2293370
TIMMDC1
0.882 0.160 3 119501087 intron variant G/A snv 0.18 3
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 3
rs4679904 0.925 0.080 3 160623108 intergenic variant C/G;T snv 2
rs860413 0.925 0.080 5 35942940 upstream gene variant A/C snv 0.23 2