Disease: Asthma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11465553
IL17F
0.925 0.120 6 52236960 missense variant C/T snv 3.0E-02 3.0E-02 2
rs512625
ADAM33
0.925 0.120 20 3667731 upstream gene variant A/G;T snv 2
rs528557
ADAM33
0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29 6
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs2787094
ADAM33
0.851 0.160 20 3668514 3 prime UTR variant C/G snv 0.71 4
rs628977
ADAM33
0.851 0.160 20 3669074 intron variant T/C snv 0.65 4
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs11584340
FLG ; FLG-AS1
0.827 0.200 1 152313454 missense variant G/A snv 0.27 0.19 5
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs5743293
NOD2
0.807 0.200 16 50729868 frameshift variant C/-;CC delins 7
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 4
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 11