Disease: Asthma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs6927172 0.851 0.120 6 137681038 intron variant C/A;G;T snv 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 6
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs4646536
CYP27B1
0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1050501
FCGR2B
0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 9