Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs223498
MANBA
1.000 0.040 4 102730805 intron variant A/C snv 0.59 1
rs7691507 1.000 0.040 4 55076834 intron variant T/C snv 0.28 1
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs10213865
LOC105374724 ; IL7R
0.827 0.120 5 35857748 intron variant A/C;T snv 5
rs4921492 0.925 0.120 5 159405269 intron variant C/A;G snv 2
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 11
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 10
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 10
rs9271770 0.776 0.120 6 32626471 upstream gene variant G/A snv 0.76 10
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 8
rs3177928
HLA-DRA
0.882 0.120 6 32444658 3 prime UTR variant G/A snv 0.13 8
rs3817963
TSBP1-AS1 ; BTNL2
0.776 0.360 6 32400310 intron variant T/C snv 0.25 8
rs6910071
TSBP1 ; TSBP1-AS1
0.790 0.320 6 32315077 intron variant A/G snv 0.14 7
rs7194
HLA-DRA
0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 7
rs615672
HLA-DRB1
0.851 0.240 6 32606394 intergenic variant G/A;C snv 6