Disease: Ankylosing spondylitis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2026029
FNDC3A
0.827 0.120 13 49021195 intron variant A/G snv 0.58 5
rs2042011 0.827 0.120 8 128215706 upstream gene variant A/G snv 0.39 5
rs2145623 0.827 0.120 14 35370030 intergenic variant G/C snv 0.32 5
rs2234161
TNFRSF14
0.827 0.120 1 2559766 non coding transcript exon variant C/T snv 4.1E-05; 0.55 0.58 5
rs2328530
CDKAL1
0.827 0.120 6 20643496 intron variant G/A snv 0.85 5
rs2357623 0.827 0.120 16 50660100 upstream gene variant A/G snv 0.71 5
rs2549803
ERAP1
0.827 0.120 5 96839226 intron variant C/T snv 0.27 5
rs2666218
ASAP2
0.827 0.120 2 9262859 intron variant A/G snv 0.32 5
rs27044
ERAP1 ; LOC102724748
0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 5
rs2779255 0.827 0.120 17 27810514 intron variant C/T snv 0.53 5
rs2823288 0.827 0.120 21 15448569 intron variant G/A snv 0.22 5
rs28550029
SKAP2
0.827 0.120 7 26832962 intron variant C/A;T snv 5
rs28701841
ATG5 ; PRDM1
0.827 0.120 6 106082455 intron variant G/A snv 7.6E-02 5
rs2910686
ERAP2 ; ERAP1
0.827 0.120 5 96916885 intron variant T/C snv 0.42 5
rs3118471
IL2RA
0.827 0.120 10 6060794 intron variant A/G snv 0.24 5
rs3124998
NOTCH1
0.827 0.120 9 136494980 3 prime UTR variant C/T snv 3.0E-02 5
rs34670647 0.827 0.120 16 30159695 regulatory region variant T/- delins 5
rs34804116 0.827 0.120 5 73244023 intron variant C/A snv 0.41 5
rs35300242
ATG16L1
0.827 0.120 2 233260144 intron variant G/A;C snv 5
rs35320439
GAL3ST2
0.827 0.120 2 241797926 intron variant T/C snv 0.44 5
rs353339 0.827 0.120 5 40201698 regulatory region variant C/A snv 0.24 5
rs3806308
RNF186
0.827 0.120 1 19816373 intron variant C/T snv 0.36 5
rs4456788
GATD3A
0.827 0.120 21 44196441 intron variant G/A snv 5
rs4655215 0.827 0.120 1 19811221 upstream gene variant T/C snv 0.68 5
rs4672505 0.827 0.120 2 62333197 regulatory region variant A/C;G;T snv 5