Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1362834154
IL4R
0.925 0.080 16 27363681 missense variant C/T snv 8.0E-06 7.0E-06 2
rs1805014
IL4R
0.851 0.080 16 27363708 missense variant T/C snv 7.4E-03 1.4E-02 4
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs2233407
NFKBIA
0.882 0.080 14 35405317 upstream gene variant T/A;C snv 3
rs4523
TBXA2R
0.776 0.280 19 3595796 missense variant A/G snv 0.56 0.66 8
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 10
rs73985228
ORMDL3
0.882 0.080 17 39922412 3 prime UTR variant G/C;T snv 3
rs4065275
ORMDL3
0.807 0.160 17 39924612 intron variant A/G;T snv 0.56 6
rs12603332
LOC112268187 ; ORMDL3 ; LRRC3C
0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 7
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs2715555
TOP2A
0.925 0.080 17 40388372 downstream gene variant G/A snv 9.5E-02 2
rs2664538
MMP9
0.827 0.200 20 46011586 missense variant A/G snv 6
rs17577
SLC12A5-AS1 ; MMP9
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs4794067
TBX21
0.807 0.280 17 47731462 upstream gene variant T/A;C snv 0.25 7
rs11650354
TBX21
1.000 0.080 17 47744726 intron variant C/A;T snv 0.16 0.15 1
rs16947078 0.925 0.080 17 47748134 downstream gene variant A/G;T snv 2
rs41347648
CYSLTR2
0.882 0.080 13 48707418 missense variant A/G snv 1.7E-02 1.7E-02 3
rs4559
NAB2 ; STAT6
0.882 0.080 12 57095865 3 prime UTR variant C/T snv 0.59 3
rs324015
STAT6
0.827 0.120 12 57096317 3 prime UTR variant T/C snv 0.76 5
rs324011
STAT6
0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs71802646
STAT6
0.882 0.080 12 57111290 5 prime UTR variant ACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACAC;ACACACACACACACACACACACACAC delins 0.32 3
rs569108
MS4A2
0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs533116 0.925 0.120 11 60860110 upstream gene variant C/T snv 0.28 2
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7