Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs501764
GATA3-AS1 ; GATA3
1.000 0.120 10 8051071 non coding transcript exon variant G/T snv 0.87 0.86 1
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 4
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs6928977
AHI1
0.925 0.120 6 135305210 intron variant T/G snv 0.70 2
rs3093998 1.000 0.120 6 31517397 downstream gene variant C/A snv 0.70 1
rs1432295
LINC01185
1.000 0.120 2 60839531 intron variant G/A snv 0.69 1
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs3806624
EOMES
0.925 0.200 3 27723132 upstream gene variant A/G snv 0.61 2
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs7111520
POU2AF1
1.000 0.120 11 111378886 intron variant G/A snv 0.58 1
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 6
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs752427
PVT1
1.000 0.120 8 127967762 intron variant C/T snv 0.55 1
rs4733809
PVT1
1.000 0.120 8 127977046 intron variant C/T snv 0.54 1
rs2608053
PVT1
1.000 0.120 8 128063586 intron variant T/C snv 0.50 1
rs805294
LY6G6C ; MPIG6B
0.882 0.240 6 31720440 intron variant A/G snv 0.48 3
rs707928
VWA7
0.827 0.320 6 31774813 intron variant A/G snv 0.47 5