Disease: White Blood Cell Count procedure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9
rs201950044 1 161639782 intergenic variant G/T snv 5
rs2208568
LOC105373215 ; LINC02768
1 235926855 intergenic variant T/A;C;G snv 5
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs34293785 1 65671509 intergenic variant T/C snv 4
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 8
rs3917914
CSF3R
1 36482287 intron variant G/A;T snv 5
rs3917932
CSF3R
1 36478315 intron variant C/G snv 0.59 5
rs41313381
ADGRL4
1 78946283 missense variant C/A;T snv 1.9E-02; 3.3E-05 4
rs4844622
MIR29B2CHG
1 207860984 intron variant C/T snv 0.19 4
rs663045
SLC25A24
1 108200437 5 prime UTR variant G/C snv 0.55 5
rs7537229 1 56440602 intron variant G/A snv 0.92 4
rs7550207
CADM3-AS1 ; ACKR1
1 159205095 intron variant T/C snv 0.19 5
rs9436747
LEPR
1 65445924 intron variant T/C snv 0.56 5
rs10206089 2 61476184 intron variant G/A snv 4
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs13033745
MEIS1 ; MEIS1-AS3
2 66433271 intron variant G/T snv 0.67 2
rs139707092
SPC25 ; NOSTRIN
2 168850753 intron variant TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT delins 5
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 5
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs4952073
EHD3 ; CAPN14
2 31235115 intron variant T/C;G snv 2