Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs2280883
FOXP3
0.827 0.280 X 49252667 intron variant T/C snv 0.30 9
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs12663103
GPSM3
0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs2517459 0.882 0.160 6 30929245 downstream gene variant T/C snv 0.74 6
rs6906021
HLA-DQB1-AS1
0.827 0.320 6 32658534 upstream gene variant T/C snv 0.47 6
rs2647050 0.882 0.240 6 32701990 downstream gene variant T/C snv 0.36 4
rs3129720 0.851 0.280 6 32695854 intergenic variant T/C snv 0.76 4
rs4821124 0.851 0.240 22 21625000 downstream gene variant T/C snv 0.19 4
rs1358379
LINC00472 ; MIR30A
0.882 0.160 6 71403739 intron variant T/C snv 6.2E-02 3
rs1439490 0.882 0.120 22 21351147 upstream gene variant T/C snv 3
rs246871
ITK ; MED7
0.882 0.160 5 157158243 intron variant T/C snv 0.42 3
rs6710479
LOC105373977 ; PDCD1
0.882 0.200 2 241855866 intron variant T/C snv 0.51 3
rs12133337
CD247
0.925 0.160 1 167483453 intron variant T/C snv 0.17 2
rs1426981647
CHEK2
0.925 0.200 22 28710038 missense variant T/C snv 4.0E-06 2
rs1431403
HLA-DPB1 ; HLA-DPA1
0.925 0.200 6 33079254 intron variant T/C snv 0.37 2
rs3130188
HLA-DPB1
0.925 0.200 6 33089399 3 prime UTR variant T/C snv 0.38 2
rs370229832
F2
0.925 0.080 11 46739293 missense variant T/C snv 3.2E-05 6.3E-05 2
rs3763355
HLA-DOB
0.925 0.200 6 32819105 intron variant T/C snv 5.2E-02 2
rs7000921 0.925 0.080 8 20535695 intergenic variant T/C snv 0.30 2
rs9276427
HLA-DQA2
0.925 0.120 6 32744080 intron variant T/C snv 0.57 2