Disease: Neutrophil count (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 7
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs10138752
RAD51B
14 68713254 intron variant C/T snv 8.8E-02 5
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs12542907 8 67900953 intergenic variant C/G snv 0.29 5