Disease: Psoriasis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
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
rs11098964
ANTXR2
0.827 0.120 4 79966815 intron variant A/G;T snv 5
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 8
rs11306716 0.827 0.120 2 203843041 intergenic variant T/-;TT delins 5
rs113994136
STAT3
0.827 0.240 17 42329642 missense variant C/A;T snv 7
rs11574938
ITGAL
0.827 0.120 16 30474072 missense variant G/A;C snv 0.62 6
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 8
rs11750385
LINC02213
0.827 0.120 5 10521556 intron variant G/A;T snv 5
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs1267499
LOC101928354
0.807 0.160 6 14715651 intron variant T/A;C snv 6
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 7
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs1333062
ITLN1
0.807 0.200 1 160876494 downstream gene variant T/C;G snv 6
rs141992399
CARD9 ; DNLZ
0.827 0.120 9 136365140 splice donor variant C/G;T snv 3.3E-03; 4.0E-06 5
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs196941
ERN1
0.827 0.120 17 64069832 non coding transcript exon variant G/C;T snv 5