Disease: Eczema
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs3024971
STAT6
0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 7
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 5
rs1811069
YDJC
1.000 0.040 22 21627765 upstream gene variant T/A;G snv 4
rs114269697
JAK1
1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 3
rs71368508
LOC105371498
1.000 0.040 17 4618178 downstream gene variant C/A snv 1.7E-02 3
rs11242709 1.000 0.040 6 209159 upstream gene variant C/T snv 0.19 2
rs11539209
ZDHHC12 ; PKN3
1.000 0.040 9 128721272 missense variant T/A;C snv 7.4E-02 2