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
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 10
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51 6
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 5
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs218264 4 54542708 intergenic variant A/G;T snv 5
rs9402686
LOC105378010
6 135106679 upstream gene variant G/A snv 0.20 5
rs9804550 11 5164863 intergenic variant T/A;C snv 5