Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs9469220 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 5
rs3892710 0.851 0.240 6 32715085 upstream gene variant C/T snv 0.22 4
rs9268542 0.851 0.280 6 32416944 intergenic variant A/G snv 0.35 4
rs2395163 0.882 0.160 6 32420032 intergenic variant T/C snv 0.17 3
rs70993900 0.882 0.080 6 32618381 intergenic variant C/- delins 4.8E-02 3
rs9275184 0.882 0.200 6 32686937 regulatory region variant T/C snv 9.1E-02 3
rs9275390 0.882 0.120 6 32701379 downstream gene variant T/C snv 0.30 3
rs7454108 0.925 0.120 6 32713706 upstream gene variant T/C snv 9.1E-02 2
rs1074532 1.000 0.080 4 65791342 intergenic variant A/G snv 0.30 1
rs11218708 1.000 0.080 11 122601355 regulatory region variant G/A snv 0.19 1
rs28483633 1.000 0.080 6 32657097 upstream gene variant C/A snv 2.2E-02 1
rs482759 1.000 0.080 6 32227240 upstream gene variant A/G;T snv 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1129055
CD86
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs5742909
CTLA4
0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs6941112
CYP21A2 ; STK19
0.882 0.120 6 31978837 intron variant G/A snv 0.25 3
rs12660382
HCP5
0.882 0.200 6 31475546 intron variant C/T snv 0.19 3
rs2395488
HCP5
0.882 0.160 6 31478132 non coding transcript exon variant A/G snv 0.34 3
rs2244839
HCP5 ; HCG26
0.882 0.200 6 31470591 non coding transcript exon variant G/A;T snv 3
rs1051336
HLA-DRA
0.925 0.120 6 32444815 3 prime UTR variant G/A;C snv 0.15 2
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 10