Disease: Ankylosing spondylitis
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2310173 0.925 0.080 2 102047167 intron variant T/C;G snv 2
rs6871626 0.851 0.160 5 159399784 intron variant C/A;G snv 0.29 3
rs7282490
GATD3A
0.882 0.080 21 44195858 intron variant G/A;T snv 4
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
rs10750899 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 5
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
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
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
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs11190133 0.827 0.120 10 99518968 intergenic variant C/T snv 0.26 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs11221322
ETS1
0.827 0.120 11 128476898 intron variant T/C snv 0.13 5
rs11306716 0.827 0.120 2 203843041 intergenic variant T/-;TT delins 5
rs114202211
HIPK1
0.827 0.120 1 113943285 intron variant T/C snv 8.1E-03 5
rs116046827
BSN
0.827 0.120 3 49618715 intron variant T/C snv 8.6E-03 5
rs11616188 0.827 0.120 12 6393576 upstream gene variant G/A snv 0.30 5
rs11624293
LINC01147
0.827 0.120 14 88022477 intron variant T/C snv 0.13 5