Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1570884
RCBTB1
13 49547375 intron variant A/G snv 0.58 4
rs1586068
IKZF2
2 213033508 intron variant A/G snv 0.81 2
rs1754541
LOC101928334
1 101160327 intergenic variant A/G snv 0.25 2
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 3
rs2296618
PTPRC
1 198697103 intron variant A/G snv 0.21 2
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
rs25884
CSF2
5 132076545 upstream gene variant A/G snv 0.31 2
rs28567906
RUNX1
21 34911514 intron variant A/G snv 0.16 2
rs35249183 1 12039288 upstream gene variant A/G snv 6.4E-02 2
rs35914442
CHD7
8 60724328 intron variant A/G snv 0.17 2
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs3755397
FARP2
0.925 0.120 2 241355498 upstream gene variant A/G snv 6.8E-02 4
rs410867 19 16316300 intron variant A/G snv 0.32 2
rs41369048
HLX-AS1 ; HLX
1 220878224 intron variant A/G snv 9.7E-02 2
rs4328821 3 128597592 intergenic variant A/G snv 0.13 2
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs511515
GGNBP1 ; BAK1
6 33573730 3 prime UTR variant A/G snv 0.73 2
rs55905691
WDR36
5 111090287 intron variant A/G snv 0.13 2
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03 5
rs5758297
ZC3H7B
22 41324693 intron variant A/G snv 0.41 2
rs634534
FOSL1
11 65897785 intron variant A/G snv 0.42 2