Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10830123
NPS
1.000 0.080 10 127551386 intron variant G/C snv 0.29 1
rs4751440
NPS
0.925 0.120 10 127552592 missense variant G/A;C snv 1.6E-05; 9.4E-02 3
rs13277355 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 3
rs7927044 0.925 0.080 11 127891771 intergenic variant G/A snv 2.3E-02 2
rs55743914
PTPRK
0.882 0.160 6 127972417 intron variant C/T snv 0.18 3
rs11412402
EEFSEC
0.925 0.080 3 128194003 intron variant -/T ins 0.65 2
rs140522418
LOC107984408
0.925 0.080 11 128302942 intergenic variant A/-;AA delins 2
rs850637 0.925 0.080 X 13005622 intergenic variant G/A snv 0.43 2
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs3749833
IRF1-AS1
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23 4
rs2299012
RAD50
0.925 0.080 5 132581248 intron variant A/C;T snv 2
rs6871536
RAD50 ; TH2LCRR
0.827 0.160 5 132634182 intron variant T/C snv 0.24 5
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs1220579705
IL4
1.000 0.080 5 132674079 missense variant C/T snv 1
rs17690965
KIF3A
0.925 0.160 5 132694975 3 prime UTR variant C/G snv 0.57 2
rs2051809
KIF3A
1.000 0.080 5 132721182 intron variant A/C snv 0.58 1
rs113010607
SEPTIN8
0.925 0.080 5 132770006 intron variant T/C snv 0.21 2
rs2069885
IL9
0.851 0.120 5 135892476 missense variant G/A;C snv 0.11 5
rs1859430
IL9
0.925 0.080 5 135894824 intron variant G/A snv 0.20 2
rs149647891
PDE7B
1.000 0.080 6 136006932 intron variant C/T snv 1.5E-02 2
rs117137535
ARRDC1
0.882 0.120 9 137605991 intron variant G/A snv 2.7E-02 3
rs6927172 0.851 0.120 6 137681038 intron variant C/A;G;T snv 5