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
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs77940566 6 42542864 intergenic variant A/C snv 0.21 2
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs8017228
STXBP6
14 24980020 intron variant A/C;G snv 2
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs143699489 3 141208279 intergenic variant A/G snv 0.22 4
rs2338224 5 72432861 intergenic variant A/G snv 0.85 5
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs4328821 3 128597592 intergenic variant A/G snv 0.13 3
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 8
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03 6
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs2856451
TNXB
6 32043581 intron variant A/G;T snv 0.59 3
rs60606273 15 64362768 intron variant A/T snv 0.84 5
rs7846314
CHD7
8 60738272 intron variant A/T snv 0.27 5
rs34762051 17 40007650 downstream gene variant AA/-;A;AAA delins 0.31 5
rs34061361
FLT3
13 28044450 intron variant AAA/-;A;AA;AAAA delins 5
rs147694761
NPC1
18 23571654 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 5
rs238914
ZBTB16
11 114113387 intron variant C/A snv 0.45 5