Disease: Ankylosing spondylitis
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 5
rs2227551
PLAU
0.827 0.120 10 73909432 intron variant G/C;T snv 6
rs2310173 0.925 0.080 2 102047167 intron variant T/C;G snv 2
rs2497318 0.827 0.120 10 92672243 upstream gene variant C/A;T snv 6
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 6
rs28550029
SKAP2
0.827 0.120 7 26832962 intron variant C/A;T snv 5
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs34670647 0.827 0.120 16 30159695 regulatory region variant T/- delins 5
rs35300242
ATG16L1
0.827 0.120 2 233260144 intron variant G/A;C snv 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs4456788
GATD3A
0.827 0.120 21 44196441 intron variant G/A snv 5
rs4672505 0.827 0.120 2 62333197 regulatory region variant A/C;G;T snv 5
rs4812833
LINC01620
0.827 0.120 20 44440356 intron variant G/A;C snv 5
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs4921482
LOC285626
0.807 0.120 5 159337470 intron variant T/C;G snv 6
rs4946717
PRDM1
0.827 0.120 6 106026874 intron variant C/A;G;T snv 6
rs4971079 0.827 0.120 1 155157915 intergenic variant G/A;C snv 5
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 6