Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs987106
IL7R
1.000 0.080 5 35875491 non coding transcript exon variant A/T snv 0.49 0.53 1
rs9695310
DDX58
0.851 0.120 9 32464137 intron variant G/C snv 0.52 4
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 6
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs944459
ESR2
1.000 0.080 14 64232640 3 prime UTR variant C/T snv 1.1E-02 1
rs9380516 0.925 0.120 6 35534425 TF binding site variant T/C snv 0.85 2
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9277535
HLA-DPB1
0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs9104
BTN3A2
1.000 0.080 6 26377921 3 prime UTR variant G/A snv 0.16 1
rs910049
TSBP1-AS1 ; TSBP1
0.776 0.400 6 32347950 intron variant T/C snv 0.76 8
rs893051
CLDN1
0.807 0.400 3 190321812 intron variant G/A;C snv 7
rs8878
ART3 ; CXCL10
0.827 0.280 4 76021147 3 prime UTR variant A/C;G snv 5
rs884000
LOC105373847
0.925 0.120 2 205815673 regulatory region variant C/A snv 0.71 2
rs879097453
GSTK1 ; LOC105375545
1.000 0.080 7 143265168 missense variant G/A snv 4.1E-06 1
rs878859113
CD24
0.763 0.360 6 106971734 missense variant G/A snv 0.35 11
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs868
TGFBR1
0.851 0.160 9 99149374 3 prime UTR variant A/G snv 0.17 4
rs854625
CCL15-CCL14 ; LOC107985068 ; CCL15
1.000 0.080 17 36001422 missense variant G/A;T snv 2
rs8191664
NEIL2
0.807 0.200 8 11786044 missense variant G/A;C;T snv 4.0E-05; 3.8E-02 7
rs8105790 0.925 0.160 19 39241861 upstream gene variant T/C snv 0.20 2