Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs3129878
HLA-DRA
0.807 0.360 6 32440958 intron variant A/C snv 0.30 6
rs9268644
HLA-DRA
0.827 0.360 6 32440267 intron variant A/C snv 0.68 5
rs1264320
DDR1
0.882 0.400 6 30893223 intron variant C/T snv 0.32 0.28 3
rs3128965
HLA-DPB1
0.882 0.280 6 33088122 3 prime UTR variant G/A snv 0.14 3
rs369252
OBSCN
0.882 0.400 1 228344451 intron variant T/G snv 0.74 3
rs1059288
RGL2 ; TAPBP
0.882 0.320 6 33299895 3 prime UTR variant A/G snv 0.60 3
rs2071888
TAPBP
0.882 0.320 6 33305078 missense variant G/C snv 0.56 0.60 3
rs17048175 0.925 0.240 2 114156886 intergenic variant T/C snv 0.19 2
rs4647376
FANCC
0.925 0.400 9 95297574 intron variant T/G snv 0.72 2
rs1042151
HLA-DPB1 ; HLA-DPA1
0.925 0.240 6 33080884 missense variant A/G snv 0.18 0.25 2
rs1188722
OBSCN
0.925 0.240 1 228276575 missense variant T/C snv 0.68 0.70 2
rs16840208
ST3GAL6 ; DCBLD2
0.925 0.240 3 98799533 missense variant C/T snv 2.1E-02 1.2E-02 2
rs3816491
ANXA4
1.000 0.240 2 69821402 intron variant C/G;T snv 1
rs1371687
DCBLD2
1.000 0.240 3 98886146 intron variant A/G snv 0.31 1
rs7615856
DCBLD2
1.000 0.240 3 98869133 intron variant C/T snv 0.36 1
rs828621
DCBLD2
1.000 0.240 3 98824818 intron variant T/A snv 0.35 1
rs8833
DCBLD2 ; ST3GAL6
1.000 0.240 3 98796725 3 prime UTR variant C/T snv 0.30 1
rs870830
GSDMB
1.000 0.240 17 39912120 intron variant G/A;C snv 1
rs1264307
GTF2H4 ; VARS2
1.000 0.240 6 30912980 intron variant G/A snv 0.28 1
rs386699871
HLA-DPB1 ; HLA-DPA1
1.000 0.240 6 33080884 missense variant ATG/GTA mnv 1
rs2074261
ILVBL
1.000 0.240 19 15115800 non coding transcript exon variant C/A snv 0.66 0.70 1
rs10780946
LOC101927086 ; TRPM3
1.000 0.240 9 70548684 intron variant T/C snv 0.48 1