Disease: Ankylosing spondylitis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10775412
KSR1
0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs1551399
LOC105375746
0.827 0.120 8 125527723 intron variant A/C snv 0.46 5
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs61802846
FCGR2A
0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 5
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs714830
CDKAL1
0.827 0.120 6 20624151 intron variant A/C;G snv 0.13 5
rs7195296 0.827 0.120 16 11655918 intergenic variant A/C;G snv 5
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs4672505 0.827 0.120 2 62333197 regulatory region variant A/C;G;T snv 5
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs11691685
TEX41
0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02 5
rs12075255
IL19
0.827 0.120 1 206788283 intron variant A/G snv 0.74 5
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12694846
SP140
0.827 0.120 2 230283413 intron variant A/G snv 0.20 5
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 6
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs17229679
LOC105373831
0.827 0.120 2 198696033 intron variant A/G snv 3.0E-02 5
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32