Disease: Allergic Reaction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
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
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 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
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 4
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 4
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 3
rs1057258
INPP5D
2 233206983 3 prime UTR variant C/T snv 0.30 3
rs13416555
LINC00299
1.000 0.080 2 8301605 intron variant C/A;G snv 3
rs346835
LINC00299
2 8298563 intron variant C/T snv 0.39 3
rs6021268
NFATC2
20 51524602 intron variant T/C snv 5.8E-02 3
rs697852
ITPKB
1 226727033 intron variant G/A snv 0.82 3
rs71368508
LOC105371498
1.000 0.040 17 4618178 downstream gene variant C/A snv 1.7E-02 3
rs9889262
ZNF652
17 49320708 intron variant T/A snv 0.28 3
rs1997502
IL1RL2
2 102227789 intron variant A/G;T snv 2