Disease: Autoimmune Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 4
rs906868 0.925 0.120 2 30225478 intergenic variant G/T snv 0.53 4
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs150240657
AGBL2
0.925 0.120 11 47682026 missense variant G/A snv 8.7E-05 3.6E-04 3
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs147846074
AIRE
0.925 0.200 21 44289743 missense variant C/G;T snv 1.2E-05; 3.2E-05; 4.0E-06 3
rs1800520
AIRE
0.851 0.200 21 44290023 missense variant C/A;G;T snv 0.14; 8.3E-06 5
rs6859219
ANKRD55
0.925 0.160 5 56142753 intron variant C/A snv 0.20 4
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs1310182
AP4B1-AS1 ; PTPN22
0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2488457
AP4B1-AS1 ; PTPN22
0.763 0.480 1 113872746 intron variant G/A;C snv 11
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11