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
rs35667974
IFIH1
0.776 0.280 2 162268127 missense variant T/C snv 1.1E-02 1.2E-02 6
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 5
rs141992399
CARD9 ; DNLZ
0.827 0.120 9 136365140 splice donor variant C/G;T snv 3.3E-03; 4.0E-06 5
rs1001007
CCR5AS
0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs1004234
LINC02863 ; IRF1-AS1
0.827 0.120 5 132421409 intron variant A/G;T snv 5
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 5
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15 5
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10750899 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 5
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs10761648
ZNF365
0.827 0.120 10 62594503 intron variant C/T snv 0.20 5
rs10775412
KSR1
0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs10800314 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 5
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10870077
CARD9
0.827 0.120 9 136369439 intron variant C/G snv 0.38 5
rs10889676
IL23R
0.827 0.120 1 67256884 intron variant C/A;T snv 5
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 5
rs11098964
ANTXR2
0.827 0.120 4 79966815 intron variant A/G;T snv 5
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8