Disease: Asthma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs2787094
ADAM33
0.851 0.160 20 3668514 3 prime UTR variant C/G snv 0.71 4
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
rs628977
ADAM33
0.851 0.160 20 3669074 intron variant T/C snv 0.65 4
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs563558831
CYP2B6
0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06 11
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 11
rs11584340
FLG ; FLG-AS1
0.827 0.200 1 152313454 missense variant G/A snv 0.27 0.19 5
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 4
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs3021097
IL10 ; IL19
0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65