Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4918
AHSG
0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 11
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
rs2308327
MGMT
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02 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
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 7
rs182123615
JAK2 ; INSL6
0.807 0.200 9 5070058 splice region variant T/C snv 3.6E-04 1.1E-03 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
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 7
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs11039155
NR1H3
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12 6
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
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 5