Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10127456
FHAD1 ; FHAD1-AS1
0.925 0.120 1 15327376 non coding transcript exon variant G/A snv 0.25 2
rs11793049
ZNF618
0.925 0.120 9 114011589 intron variant A/G;T snv 2
rs12068753 1.000 0.120 1 159722747 intergenic variant T/A snv 0.15 2
rs12210919
MDGA1
0.925 0.120 6 37677736 intron variant T/C snv 6.8E-02 2
rs12900413
MESP2
0.925 0.120 15 89777808 intron variant A/G snv 0.27 2
rs17136627
LOC101927078 ; KCNN2
0.925 0.120 5 114463289 intron variant C/T snv 7.5E-02 2
rs17667932
MED30
1.000 0.120 8 117537137 intron variant T/C snv 7.5E-02 2
rs17782904
SETBP1
0.925 0.120 18 44733745 intron variant G/A snv 0.18 2
rs2409781
BLK
0.925 0.120 8 11502048 intron variant T/A;C snv 2
rs10082659
LDLRAD3
1.000 0.120 11 36122428 intron variant G/T snv 0.42 1
rs10100215
BLK
1.000 0.120 8 11504763 intron variant G/T snv 0.26 1
rs10866845
LOC102723395 ; EBF2
1.000 0.120 8 25850751 synonymous variant T/C snv 0.42 0.49 1
rs1113452
FSD2
1.000 0.120 15 82805465 intron variant G/A snv 3.5E-05 1
rs11250141
BLK
1.000 0.120 8 11514632 intron variant G/A snv 0.48 1
rs11340705
LINC00690
1.000 0.120 3 16526578 intron variant AA/-;A;AAA delins 1
rs1150793
MSH5 ; MSH5-SAPCD1
1.000 0.120 6 31749919 intron variant A/G snv 0.11 1
rs11734
ZSCAN25
1.000 0.120 7 99632145 3 prime UTR variant G/A;C snv 1
rs11990277
BLK
1.000 0.120 8 11514576 intron variant T/C snv 0.23 1
rs12722477
HLA-G
1.000 0.120 6 29828599 missense variant C/A snv 0.14 0.14 1
rs13256690 1.000 0.120 8 11481059 non coding transcript exon variant G/A;C;T snv 1
rs1438386
SMAD3
1.000 0.120 15 67115561 intron variant G/A snv 0.51 1
rs1478887
BLK
1.000 0.120 8 11498471 intron variant C/T snv 0.64 1
rs1478895
BLK
1.000 0.120 8 11495826 intron variant G/C snv 0.83 1
rs1478900
BLK
1.000 0.120 8 11490151 intron variant C/G;T snv 1
rs1478901
BLK
1.000 0.120 8 11490324 intron variant G/C snv 0.25 1