Disease: Allergic rhinitis (disorder)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs8076131
ORMDL3
0.790 0.200 17 39924659 intron variant G/A;C snv 11
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 7
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 5
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 4
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 4
rs10519067
RORA
0.925 0.120 15 60776148 intron variant G/A snv 0.20 3
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52 3
rs7717955
IL7R
0.925 0.200 5 35862739 intron variant C/T snv 0.23 3
rs9775039 0.925 0.120 9 6177453 intergenic variant G/A snv 0.20 3
rs11169225
AQP2 ; LOC101927318
1.000 0.120 12 49951888 intron variant T/A snv 0.13 2
rs11644510
CLEC16A
1.000 0.120 16 11183501 downstream gene variant C/T snv 0.39 2
rs13395467
LINC00299
1.000 0.120 2 8311368 intron variant A/G snv 0.24 2
rs148505069 1.000 0.120 4 122496409 intergenic variant A/G snv 0.29 2
rs2070902
FCER1G
1.000 0.120 1 161217875 intron variant C/T snv 0.31 2
rs34004019
HLA-DQB1-AS1
1.000 0.120 6 32658626 upstream gene variant A/G snv 0.29 2
rs3787184
NFATC2
1.000 0.120 20 51541298 intron variant A/G snv 0.17 2
rs61977073
TTC6
1.000 0.120 14 37682050 intron variant A/G snv 0.16 2