Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1328454
SLC9A8
0.827 0.120 20 49823486 intron variant T/C snv 0.57 5
rs4812833
LINC01620
0.827 0.120 20 44440356 intron variant G/A;C snv 5
rs79493594
PKIG
0.827 0.120 20 44561731 intron variant C/T snv 2.1E-02 5
rs6017342
LINC01620
0.925 0.120 20 44436388 non coding transcript exon variant A/C snv 0.62 3
rs6062504
ZGPAT
0.925 0.040 20 63717555 intron variant A/G;T snv 3
rs6088765
MMP24-AS1-EDEM2 ; MMP24OS ; PROCR
1.000 0.040 20 35211477 intron variant T/G snv 0.54 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 16
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 11
rs2305764
MYO9B
0.776 0.360 19 17203024 non coding transcript exon variant G/A snv 0.52 0.50 10
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs1457092
MYO9B
0.790 0.320 19 17193427 intron variant C/A snv 0.44 8
rs4740
EBI3
0.827 0.240 19 4236999 missense variant G/A snv 0.34 0.39 8
rs34436714
NLRP12
0.851 0.120 19 53824059 missense variant C/A;T snv 0.22 7
rs679574
FUT2 ; LOC105447645
0.827 0.120 19 48702851 intron variant C/G snv 0.45 7
rs1545620
MYO9B
0.827 0.080 19 17192965 missense variant T/A;G snv 1.3E-05; 0.52 6