Disease: Asthma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050153
TFRC
0.925 0.120 3 196049444 3 prime UTR variant G/A snv 2
rs10791824
OVOL1-AS1 ; OVOL1
0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs1214598
LOC101928512 ; CD247
0.925 0.120 1 167457187 non coding transcript exon variant G/A;C;T snv 3
rs12186803
KIF3A
0.925 0.120 5 132704377 intron variant G/A;C snv 2
rs138726443
FLG ; FLG-AS1
0.790 0.200 1 152307547 stop gained G/A;C;T snv 2.8E-03; 4.0E-06; 1.6E-05 7
rs150597413
FLG ; FLG-AS1
0.827 0.160 1 152305146 stop gained G/A;C;T snv 3.6E-05; 4.0E-06; 1.5E-03 5
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1555549674
STAT5B
0.882 0.240 17 42223402 missense variant T/G snv 6
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1805011
IL4R
0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 8
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2390314 0.925 0.120 7 20416355 downstream gene variant A/C;T snv 3
rs2899642
RNF111
0.925 0.120 15 59030849 missense variant C/G;T snv 0.36; 1.2E-05 2
rs320995
CYSLTR1
0.851 0.240 X 78272820 missense variant G/A;C;T snv 0.73 4
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs555743307
IL4R
0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs7124842 0.882 0.160 11 76600576 intergenic variant G/A;C;T snv 3
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs941934
FLG-AS1
0.851 0.200 1 152417976 intron variant T/A;C snv 5
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614