Disease: Granulocyte count
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
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs56232812 1 27859995 intergenic variant A/C snv 0.11 4
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs12752838 1 8853597 upstream gene variant A/G snv 0.54 4
rs1352846
GC
4 71752058 intron variant A/G snv 0.22 4
rs1570884
RCBTB1
13 49547375 intron variant A/G snv 0.58 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 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
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs73036517
MARK4 ; EXOC3L2
19 45241584 intron variant A/G snv 0.20 4
rs834603
TNS3
7 47408324 intron variant A/G snv 0.47 4
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs138488218 12 53354069 regulatory region variant A/T snv 7.6E-03 4
rs60606273 15 64362768 intron variant A/T snv 0.84 5
rs675600
LINC02210 ; LINC02210-CRHR1
17 45618793 upstream gene variant A/T snv 0.14 4
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