Disease: Asthma
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5
rs3117098
HCG23 ; TSBP1-AS1
0.851 0.280 6 32390736 non coding transcript exon variant G/A snv 0.72 4
rs3129943
TSBP1-AS1 ; TSBP1
0.851 0.240 6 32370918 intron variant A/G snv 0.26 4
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 3
rs241425
TAP2
0.925 0.160 6 32837132 intron variant A/C;G snv 2
rs404860
NOTCH4
0.925 0.160 6 32216568 non coding transcript exon variant T/C snv 0.21 2
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 2