Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 4
rs7753873
LOC107986649 ; WAKMAR2
0.882 0.320 6 137852285 intron variant A/C snv 0.18 3
rs12119179 0.925 0.200 1 67281732 downstream gene variant A/C snv 0.30 2
rs7574070
STAT4
1.000 0.200 2 191145762 intron variant A/C snv 0.55 1
rs2227981
LOC105373977 ; PDCD1
0.763 0.400 2 241851121 synonymous variant A/C;G snv 1.6E-04; 0.63 12
rs1310182
AP4B1-AS1 ; PTPN22
0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs6910516 1.000 0.200 6 31376050 non coding transcript exon variant A/C;G snv 1
rs7572482
STAT4
1.000 0.200 2 191150346 intron variant A/C;G snv 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs10863888
TRAF5
0.851 0.280 1 211329427 intron variant A/C;G;T snv 4
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs10515746
HAVCR2
0.925 0.240 5 157109557 intron variant A/C;T snv 2
rs9316059
NRAD1 ; LOC107984576
1.000 0.200 13 43912653 intron variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13