Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs324011
STAT6
0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 9
rs3745367
RETN
0.827 0.200 19 7669625 intron variant G/A snv 0.39 8
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 7
rs893051
CLDN1
0.807 0.400 3 190321812 intron variant G/A;C snv 7
rs10249788
LOC101927609 ; AHR
0.827 0.160 7 17298523 intron variant C/G;T snv 6
rs2844509
SNORD84 ; DDX39B-AS1 ; DDX39B ; ATP6V1G2-DDX39B
0.882 0.160 6 31543147 intron variant A/G snv 0.23 6
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 6
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs1343795
ZNF652
0.882 0.120 17 49334880 intron variant C/A snv 0.78 5
rs17501010
LOC107986170 ; CLDN1
0.827 0.320 3 190308865 intron variant G/T snv 0.15 5
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 5
rs2158177
TH2LCRR
0.925 0.120 5 132648366 intron variant A/G snv 0.18 5
rs2853209
ADAM33
0.827 0.200 20 3670825 intron variant T/A snv 0.41 5
rs3126085
FLG-AS1
0.851 0.280 1 152328341 intron variant G/A snv 0.29 5
rs6871536
RAD50 ; TH2LCRR
0.827 0.160 5 132634182 intron variant T/C snv 0.24 5
rs941934
FLG-AS1
0.851 0.200 1 152417976 intron variant T/A;C snv 5
rs4572450
ZNF652
0.882 0.120 17 49343367 intron variant T/C snv 0.78 4
rs4722404 0.851 0.120 7 3089155 intron variant T/C snv 0.40 4