Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs9333289
ITGAV
1.000 0.080 2 186633380 splice region variant T/A;C snv 0.25 1
rs9288516
XRCC5
0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6
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
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs9274407
HLA-DQB1
0.925 0.120 6 32665055 missense variant A/C;T snv 0.77 3
rs9272535
HLA-DQA2 ; LOC107986589 ; HLA-DQA1
0.827 0.280 6 32638979 synonymous variant G/A snv 3.0E-05 1.8E-03 7
rs9272105
HLA-DQA1
0.925 0.120 6 32632222 intron variant G/A snv 0.55 2
rs9271568 0.925 0.200 6 32622686 TF binding site variant G/A snv 0.27 2
rs9267673
C2 ; CYP21A2
0.925 0.080 6 31915902 intron variant C/A;T snv 0.12 5
rs9267665
ZBTB12 ; C2 ; CYP21A2
0.925 0.200 6 31903079 intron variant C/T snv 7.3E-02 2
rs9261204
ZNRD1ASP
0.790 0.200 6 30037466 intron variant A/G snv 0.17 9
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs9200
C6 ; LOC105374739
1.000 0.080 5 41142504 3 prime UTR variant C/A;T snv 2
rs913493
PCDH9
1.000 0.080 13 67148073 intron variant A/G snv 0.20 1
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs903934130
CCDC33
1.000 0.080 15 74318618 missense variant C/T snv 2.1E-05 1
rs897206619
HFE
0.882 0.120 6 26093128 missense variant C/T snv 3.5E-05 3
rs8971
GART
1.000 0.080 21 33511311 missense variant T/C snv 0.21 0.18 1
rs894151
C8orf37-AS1
1.000 0.080 8 95226180 intron variant T/C snv 0.39 2
rs8898
CTSB
0.925 0.120 8 11845033 3 prime UTR variant T/C snv 0.37 5
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs886039463
PTPN11
1.000 0.080 12 112489096 missense variant C/A snv 3