Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs324011
STAT6
0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 11
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
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
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
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
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 5
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs2734986
LOC105375010
0.827 0.160 6 29850791 intron variant T/C snv 0.10 5
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs707928
VWA7
0.827 0.320 6 31774813 intron variant A/G snv 0.47 5
rs11715604
NCK1
0.851 0.160 3 136870707 intron variant A/G;T snv 4
rs131821
NCAPH2
0.851 0.160 22 50511648 intron variant T/-;TT;TTT;TTTT delins 4
rs149207840
SP140
0.851 0.160 2 230279864 intron variant CTGCCTC/-;CTGCCTCCTGCCTC delins 0.15 4
rs181181503
LOC100507377
0.851 0.160 12 74276187 intron variant T/C snv 1.5E-03 4