Disease: Psoriasis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
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
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
rs1126667
ALOX12 ; ALOX12-AS1
0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
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
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 8
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 9
rs72743477
SMAD3
0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 5
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 9