Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1555525115
ANKRD11
0.851 0.360 16 89279567 frameshift variant GGCTTCGG/- delins 5
rs167769
STAT6
0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 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
rs2251396
MICA-AS1
0.827 0.240 6 31396930 upstream gene variant G/A snv 0.24 5
rs2289278
TSLP
0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02 5
rs2427837
FCER1A
0.851 0.160 1 159288755 upstream gene variant G/A snv 0.20 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
rs1057518775
KCNJ11
0.851 0.160 11 17387907 missense variant G/A;C snv 4
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 4
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
rs4982958 0.851 0.200 14 24518659 intergenic variant C/T snv 0.50 4
rs5744292
IL18
0.851 0.200 11 112143413 3 prime UTR variant T/C snv 0.16 4
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 4
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs7936562 0.882 0.160 11 76567214 intergenic variant T/C snv 0.59 4
rs9357733
EFHC1
0.851 0.160 6 52427338 intron variant A/G snv 0.19 4
rs976078 0.882 0.120 13 82963398 intron variant A/C snv 0.15 4