Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3775572
IRF2
0.925 0.120 4 184448298 intron variant G/A snv 0.82 2
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs1343795
ZNF652
0.882 0.120 17 49334880 intron variant C/A snv 0.78 5
rs6419573 1.000 0.120 2 102410643 upstream gene variant T/C snv 0.78 1
rs4572450
ZNF652
0.882 0.120 17 49343367 intron variant T/C snv 0.78 4
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 3
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs6548123
MYT1L
0.925 0.120 2 2221629 intron variant C/T snv 0.76 2
rs11205006 1.000 0.120 1 152467700 intergenic variant A/T snv 0.72 1
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs6686734
MFN2
1.000 0.120 1 12008884 intron variant T/C snv 0.71 1
rs2944542
ZNF365
0.925 0.120 10 62610240 intron variant C/G snv 0.71 2
rs793814
IRF2
0.925 0.120 4 184433820 intron variant T/A snv 0.70 2
rs444762
GATA3
0.925 0.120 10 8061297 intron variant A/C snv 0.67 2
rs3756094
IRF2
0.925 0.120 4 184429780 intron variant A/G snv 0.66 2
rs9290929
CLDN16
0.925 0.120 3 190325950 intron variant G/A snv 0.65 2
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs4363385
LOC105371446
0.925 0.120 1 153016845 upstream gene variant T/C snv 0.62 2
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs7936562 0.882 0.160 11 76567214 intergenic variant T/C snv 0.59 4
rs17690965
KIF3A
0.925 0.160 5 132694975 3 prime UTR variant C/G snv 0.57 2
rs7000782 1.000 0.120 8 80395915 intron variant T/A snv 0.54 1
rs6473227 0.925 0.120 8 80373657 intron variant C/A snv 0.54 2
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14