Disease: Asthma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs449454
NDFIP1
0.925 0.080 5 142153497 3 prime UTR variant A/G snv 0.65 0.68 3
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38 4
rs2188962
IRF1-AS1
0.882 0.160 5 132435113 intron variant C/T snv 0.29 5
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 5
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18 5
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 6
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs3764147
LACC1
0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 7
rs5743293
NOD2
0.807 0.200 16 50729868 frameshift variant C/-;CC delins 7
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs2075820
NOD1
0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs721917
SFTPD
0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19