Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs796051881
PEX5
0.807 0.440 12 7202274 frameshift variant -/A delins 9
rs34445740
SMAD3
0.925 0.080 15 67183426 intron variant -/A delins 0.29 2
rs540485182 0.925 0.080 5 110825774 intergenic variant -/A;AA;AAA delins 2
rs1799768
SERPINE1
0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs3831317
CHIT1
0.925 0.080 1 203217822 stop gained -/AGACCATGGCCCCGCCCAGTCCCT delins 2
rs10699671
NDFIP1
0.925 0.080 5 142139375 intron variant -/AGG delins 0.68 2
rs560026225 1.000 0.080 4 122134546 intergenic variant -/AT delins 1.3E-02 1
rs71266076 1.000 0.080 8 80354702 intron variant -/C;TGAGACA ins 1.4E-05 1
rs202011557 1.000 0.080 2 102297182 intergenic variant -/CAA delins 1
rs113092121
KIF11
0.925 0.080 10 92624756 intron variant -/CTCT delins 2
rs149317277
ITGB8
0.925 0.080 7 20384300 intron variant -/GAAACAAGATTCT;GAACCAAGATTCT delins 0.36 2
rs869312169
DOCK8
0.925 0.080 9 452067 frameshift variant -/T delins 3
rs11412402
EEFSEC
0.925 0.080 3 128194003 intron variant -/T ins 0.65 2
rs113612868
TCAP
1.000 0.080 17 39665182 upstream gene variant -/T ins 1
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs140522418
LOC107984408
0.925 0.080 11 128302942 intergenic variant A/-;AA delins 2
rs35204956 0.925 0.080 8 80389778 intron variant A/-;AA;AAA delins 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21 9
rs242941
MAPT-AS1 ; CRHR1 ; LINC02210-CRHR1
0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs3129878
HLA-DRA
0.807 0.360 6 32440958 intron variant A/C snv 0.30 6
rs9268644
HLA-DRA
0.827 0.360 6 32440267 intron variant A/C snv 0.68 5
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs2305482
PSMD3
0.851 0.200 17 39984674 intron variant A/C snv 0.57 4