Disease: Chronic Obstructive Airway Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11779254
CSMD1
0.925 0.080 8 4391552 intron variant G/C;T snv 2
rs2544523 0.925 0.080 2 15780199 intergenic variant T/A;C snv 2
rs25882
CSF2
0.925 0.080 5 132075767 missense variant T/C snv 0.26 0.26 2
rs3831317
CHIT1
0.925 0.080 1 203217822 stop gained -/AGACCATGGCCCCGCCCAGTCCCT delins 2
rs59569785
SOX5
0.925 0.080 12 23618801 intron variant C/T snv 0.18 2
rs6574978
LOC107984669 ; GPR65
0.925 0.080 14 88011069 synonymous variant C/T snv 0.75 0.72 2
rs9534578
LOC105370195
0.925 0.080 13 47269242 intergenic variant C/A snv 0.11 2
rs17154353
SLC26A4
0.925 0.080 7 107710182 missense variant G/A;T snv 3.7E-03; 8.0E-06 3
rs200039720
SFTPC
0.925 0.080 8 22162688 missense variant G/A snv 1.5E-04 1.0E-04 3
rs2241712
B9D2 ; TMEM91
0.882 0.120 19 41363851 intron variant C/T snv 0.71 3
rs2280091
ADAM33
0.882 0.080 20 3669587 missense variant A/G snv 0.13 0.14 3
rs3741240
LOC102723765 ; SCGB1A1
0.882 0.120 11 62419070 5 prime UTR variant G/A snv 0.34 0.32 3
rs612709
ADAM33
0.882 0.120 20 3671560 intron variant G/A snv 0.17 0.25 3
rs301819
RERE
0.882 0.120 1 8441726 intron variant A/G;T snv 4
rs4253238
KLKB1
0.925 0.080 4 186227233 intron variant C/T snv 0.59 4
rs1042711
ADRB2
0.827 0.120 5 148826785 5 prime UTR variant C/A;G;T snv 4.2E-06; 0.68 5
rs37972
GLCCI1-DT ; UMAD1 ; GLCCI1
0.851 0.160 7 7967878 3 prime UTR variant T/A;C snv 5
rs3918396
ADAM33
0.851 0.120 20 3671118 missense variant C/T snv 5.1E-05; 7.6E-02 6.7E-02 5
rs758244932
EPHX1
0.827 0.120 1 225828842 missense variant C/T snv 1.3E-04 1.0E-04 5
rs769790595
IL4R
0.827 0.120 16 27360785 missense variant G/A;C snv 2.0E-05; 4.0E-06 5
rs1974226
IL17A
0.827 0.240 6 52190537 3 prime UTR variant C/T snv 0.15 6
rs4795405
LRRC3C
0.851 0.160 17 39932164 intron variant T/A;C snv 6
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
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18 7