Disease: Allergic Reaction
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs11674302 1.000 0.080 2 102270668 intergenic variant T/C snv 0.16 2
rs11692065 1.000 0.080 2 102267515 intergenic variant C/T snv 0.15 2
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs12950743 0.925 0.160 17 39892980 intergenic variant T/C snv 0.45 3
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 2
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 2
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 2
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 2
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 3
rs7359623 0.925 0.160 17 39893336 intergenic variant C/T snv 0.44 3
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 3
rs9901146 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 3
rs9907088 0.925 0.160 17 39878863 downstream gene variant G/A snv 0.39 3
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 2
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs11078927
GSDMB
0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 2
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs2305479
GSDMB
0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 4
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs4795400
GSDMB
0.925 0.080 17 39910767 intron variant C/T snv 0.36 3