Disease: Neutrophil count (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs58548501 4 54635119 intergenic variant -/A;ATTTTTTTTTA ins 0.43 4
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
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs56232812 1 27859995 intergenic variant A/C snv 0.11 4
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs12593998
SPPL2A
15 50766432 upstream gene variant A/C;G snv 2
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs11137087 8 7048518 intergenic variant A/G snv 0.60 2
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs12752838 1 8853597 upstream gene variant A/G snv 0.54 4
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs1352846
GC
4 71752058 intron variant A/G snv 0.22 4
rs1567558
PXYLP1
3 141289281 intron variant A/G snv 0.50 2
rs1570884
RCBTB1
13 49547375 intron variant A/G snv 0.58 4
rs2251188 7 6664701 intron variant A/G snv 0.71 2
rs2338224 5 72432861 intergenic variant A/G snv 0.85 5
rs2451279
LOC112267968
6 159094045 intron variant A/G snv 0.73 2
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03 5