Disease: Psoriasis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1250546
ZMIZ1
0.925 0.080 10 79272775 intron variant A/G snv 0.36 3
rs11938228
TLR2
0.882 0.120 4 153700794 intron variant C/A;T snv 4
rs26653
ERAP1
0.882 0.080 5 96803547 missense variant C/A;G;T snv 0.64; 8.0E-06; 9.1E-04 4
rs2274907
ITLN1
0.851 0.200 1 160882036 missense variant A/G;T snv 0.66 5
rs11614178
IFNG-AS1 ; LOC107984526
0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
rs12718244
SPATA48
0.827 0.120 7 50136058 intron variant G/A snv 0.33 0.33 6
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 6
rs2050392 0.827 0.120 10 30402574 downstream gene variant G/A snv 0.45 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs34779708
CREM
0.827 0.120 10 35177257 intron variant T/G snv 0.33 6
rs3766606
PARK7
0.827 0.120 1 7962137 intron variant G/T snv 0.22 6
rs3776414
DAP
0.827 0.120 5 10689450 intron variant T/G snv 0.48 6
rs3853824
C17orf67
0.827 0.120 17 56803632 intron variant T/C snv 0.66 6
rs395157
OSMR
0.827 0.120 5 38867630 intron variant C/T snv 0.47 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs4703855 0.827 0.120 5 72398072 regulatory region variant C/T snv 0.24 6
rs4802307
PPP5C
0.827 0.120 19 46346549 upstream gene variant G/T snv 0.21 6
rs4946717
PRDM1
0.827 0.120 6 106026874 intron variant C/A;G;T snv 6