Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs3092920 0.925 0.160 X 136661832 downstream gene variant G/T snv 0.23 2
rs1129055
CD86
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs4610776
DEFA5
1.000 0.040 8 7057155 upstream gene variant A/T snv 0.26 1
rs4837656 1.000 0.040 9 119671775 intergenic variant T/C snv 0.27 1
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3092952 0.925 0.160 X 136644791 upstream gene variant A/G snv 0.29 3
rs4833079
KLF3-AS1
1.000 0.040 4 38653060 intron variant T/C snv 0.30 2
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs2278294
IMPDH1
0.882 0.080 7 128400645 non coding transcript exon variant C/T snv 0.38 3
rs9277534
HLA-DPB1
0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 7
rs9277378
HLA-DPB1 ; HLA-DPA1
0.827 0.320 6 33082502 intron variant A/G snv 0.40 5
rs2310241
IL1RL2
1.000 0.040 2 102225489 intron variant A/C snv 0.44 1
rs7251
IRF3
0.925 0.080 19 49659652 missense variant C/A;G snv 0.39 0.44 2
rs2278293
IMPDH1
0.882 0.040 7 128400698 non coding transcript exon variant C/T snv 0.47 3
rs7588571
REG3A
0.882 0.040 2 79161461 intron variant G/A snv 0.49 3
rs3004070
DAAM2 ; MOCS1
1.000 0.040 6 39902176 3 prime UTR variant T/A snv 0.51 1
rs4845618
IL6R
0.851 0.160 1 154427539 intron variant G/T snv 0.53 5
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs4364254
HPSE
0.882 0.080 4 83302560 intron variant C/T snv 0.63 3
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs6531656
KLF3
1.000 0.040 4 38682580 intron variant C/T snv 0.87 2