Disease: Asthma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs2240017
TBX21
0.925 0.160 17 47733553 missense variant C/G snv 4.9E-02 2.8E-02 2
rs3763309
TSBP1-AS1 ; BTNL2
0.882 0.160 6 32408196 upstream gene variant C/A;T snv 3
rs37972
GLCCI1-DT ; UMAD1 ; GLCCI1
0.851 0.160 7 7967878 3 prime UTR variant T/A;C snv 5
rs740347
NPSR1 ; NPSR1-AS1
0.925 0.160 7 34772690 intron variant G/A;C;T snv 2
rs881375
PHF19
0.925 0.160 9 120890620 intron variant T/C snv 0.68 2
rs9275698 0.925 0.160 6 32720196 downstream gene variant A/G snv 0.37 2
rs987870
HLA-DPA1 ; HLA-DPB1
0.851 0.160 6 33075103 intron variant A/G snv 0.19 4
rs2844482
LOC100287329 ; LTA
0.882 0.200 6 31571990 upstream gene variant C/T snv 0.15 4
rs7192
HLA-DRA
0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 7
rs9268516 0.882 0.200 6 32411712 upstream gene variant C/T snv 0.24 3
rs2647044 0.882 0.240 6 32700133 intergenic variant G/A snv 0.10 3
rs3129943
TSBP1-AS1 ; TSBP1
0.851 0.240 6 32370918 intron variant A/G snv 0.26 4
rs572527200
MMP12
0.882 0.240 11 102875064 upstream gene variant T/C snv 4
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 10
rs3117098
HCG23 ; TSBP1-AS1
0.851 0.280 6 32390736 non coding transcript exon variant G/A snv 0.72 4
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs41297579
HAVCR1
0.807 0.280 5 157059397 upstream gene variant C/T snv 0.15 6
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs1059288
RGL2 ; TAPBP
0.882 0.320 6 33299895 3 prime UTR variant A/G snv 0.60 3
rs1063355
HLA-DQB1-AS1 ; HLA-DQB1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 5
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs2071888
TAPBP
0.882 0.320 6 33305078 missense variant G/C snv 0.56 0.60 3
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10