Disease: Psoriasis vulgaris
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 14
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs2248374
ERAP1 ; ERAP2
0.851 0.120 5 96900192 splice region variant A/G snv 0.55 0.54 4
rs4683946 0.925 0.080 3 101896982 intron variant G/T snv 0.19 2