Disease: Psoriasis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 10
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 8
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs3747517
IFIH1
0.732 0.360 2 162272314 missense variant T/C snv 0.68 0.68 13
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 11
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs582757
TNFAIP3
0.776 0.320 6 137876687 intron variant C/T snv 0.70 8
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 9
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 19