Disease: Asthma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
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
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 11
rs2787094
ADAM33
0.851 0.160 20 3668514 3 prime UTR variant C/G snv 0.71 4
rs3021097
IL10 ; IL19
0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 4
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs512625
ADAM33
0.925 0.120 20 3667731 upstream gene variant A/G;T snv 2