Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs796052243
SPATA5
0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 32
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs9831894
CD86
0.882 0.120 3 122081640 intron variant A/C snv 0.31 3
rs778986
FUT3
1.000 0.080 19 5844526 missense variant A/G snv 0.84 0.84 3
rs16862780
LINC01991
0.925 0.080 3 187970052 intron variant G/A;T snv 3
rs10071761 0.925 0.080 5 40415509 intron variant T/C snv 0.31 2
rs11299600 0.925 0.080 8 128192327 regulatory region variant A/- delins 0.29 2
rs12257092 0.925 0.080 10 89023070 intergenic variant A/T snv 0.27 2
rs146583707 0.925 0.080 4 122571262 intergenic variant T/A snv 0.20 2
rs4565870 0.925 0.080 11 46328319 upstream gene variant T/C snv 0.43 2
rs67257959 0.925 0.080 19 17047335 upstream gene variant T/A;C snv 2
rs7773987
AHI1
0.925 0.080 6 135386348 intron variant C/T snv 0.60 2
rs34069391
CLEC16A
0.925 0.080 16 11067358 intron variant T/- delins 2
rs2136613
EGR2
0.925 0.080 10 62834404 intron variant C/G;T snv 2
rs2210913
FCRL3
0.925 0.080 1 157699203 intron variant C/T snv 0.56 2
rs812936
FUT3
1.000 0.080 19 5844638 missense variant G/A;C snv 0.83 2
rs1244181
GATA3
0.925 0.080 10 8049414 intron variant A/C;G snv 2
rs116041786
HLA-DQA1
0.925 0.080 6 32634619 intron variant C/T snv 2
rs8071789
IKZF3
0.925 0.080 17 39850080 intron variant C/T snv 0.47 2
rs10905875
LOC101928080
0.925 0.080 10 6131814 intergenic variant G/A;C snv 2
rs80168506
LOC107985981
0.925 0.080 2 213196729 intergenic variant A/G snv 5.1E-02 2
rs12967678
PTPN2
0.925 0.080 18 12805389 intron variant G/A snv 8.0E-02 2