Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs181206
IL27
0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24 16
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs1867277
PTCSC2 ; FOXE1
0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 10
rs3811047
IL37
0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs10818488
C5-OT1
0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 8
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs179247
TSHR
0.882 0.160 14 80966202 intron variant A/G snv 0.40 5
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs623011 0.827 0.320 17 70263305 intergenic variant A/G snv 0.74 5
rs2243289
LOC105379176 ; IL4
0.882 0.240 5 132682440 intron variant A/G snv 0.26 0.23 3
rs2893321
TNFSF13B
0.882 0.200 13 108290686 intron variant A/G snv 0.20 3
rs3093024
LOC105378122 ; CCR6
0.882 0.200 6 167119305 non coding transcript exon variant A/G snv 0.61 3
rs853326
TG
0.882 0.120 8 132897729 missense variant A/G snv 0.58 0.60 3
rs1230666
MAGI3
0.925 0.200 1 113630788 intron variant A/G snv 0.90 2
rs1269486
GATA3 ; GATA3-AS1 ; LOC107984204
0.925 0.120 10 8054236 intron variant A/G snv 0.77 2
rs16975792 0.925 0.280 17 70437584 intergenic variant A/G snv 0.26 2
rs2267873
DIO2
0.925 0.160 14 80207471 intron variant A/G snv 0.20 2
rs2274736
PTPN21
0.925 0.160 14 88472308 missense variant A/G snv 0.33; 4.0E-06 0.38 2
rs2596449
HCP5 ; HCG26
0.925 0.160 6 31470613 non coding transcript exon variant A/G snv 0.79 2
rs2618431
FAM167A
0.925 0.120 8 11466955 intron variant A/G snv 0.87 2
rs4411444
TSHR
0.925 0.120 14 80978764 intron variant A/G snv 0.43 2
rs4711332
ITPR3
0.925 0.200 6 33627622 intron variant A/G snv 0.86 2
rs6110809
MACROD2
0.925 0.120 20 15870432 intron variant A/G snv 0.67 2