Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs3138053
NFKBIA
0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 10
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 7
rs360719
IL18 ; LOC107987164 ; TEX12
0.790 0.480 11 112165426 non coding transcript exon variant A/G snv 0.25 7
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 7
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs2534657
MICB
0.882 0.200 6 31504682 intron variant C/T snv 0.15 6
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs9268403
TSBP1 ; TSBP1-AS1
0.807 0.240 6 32373696 intron variant T/C snv 0.24 6
rs9657182
IDO1
0.851 0.280 8 39908329 intron variant C/G;T snv 6
rs121964877
CDH1
0.851 0.160 16 68822081 stop gained C/G;T snv 5
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs2516513
MICB-DT
0.925 0.120 6 31479811 downstream gene variant C/T snv 0.20 5
rs2734986
LOC105375010
0.827 0.160 6 29850791 intron variant T/C snv 0.10 5
rs2763979
HSPA1B
0.827 0.360 6 31826815 upstream gene variant C/T snv 0.45 5
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs707928
VWA7
0.827 0.320 6 31774813 intron variant A/G snv 0.47 5
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs11715604
NCK1
0.851 0.160 3 136870707 intron variant A/G;T snv 4