Disease: Psoriasis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6
rs6058869
DNMT3B
0.827 0.120 20 32760944 upstream gene variant C/T snv 0.55 6
rs6062496
TNFRSF6B ; RTEL1-TNFRSF6B
0.827 0.120 20 63697746 intron variant G/A snv 0.52 6
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 6
rs6863411
NDFIP1
0.827 0.120 5 142133639 intron variant A/T snv 0.67 6
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv 6
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs7236492
NFATC1 ; LOC101927897
0.827 0.120 18 79460616 non coding transcript exon variant C/T snv 0.11 6
rs7404095
PRKCB
0.827 0.120 16 23853269 intron variant T/C snv 0.58 6
rs7608910
PUS10
0.827 0.120 2 60977721 intron variant A/G snv 0.37 6
rs925255
FOSL2 ; FLJ31356
0.827 0.120 2 28391927 intron variant C/T snv 0.38 6
rs9297145
KPNA7
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67 6
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 6
rs9889296 0.827 0.120 17 34243528 intergenic variant G/A snv 0.33 6
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 7
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 7
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 7
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 7
rs5743293
NOD2
0.807 0.200 16 50729868 frameshift variant C/-;CC delins 7
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 7
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 8
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 8