rs4857855
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4857855(C;C) |
Make rs4857855(C;T) |
Make rs4857855(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 128541707 |
is a | snp |
is | mentioned by |
dbSNP | rs4857855 |
dbSNP (classic) | rs4857855 |
ClinGen | rs4857855 |
ebi | rs4857855 |
HLI | rs4857855 |
Exac | rs4857855 |
Gnomad | rs4857855 |
Varsome | rs4857855 |
LitVar | rs4857855 |
Map | rs4857855 |
PheGenI | rs4857855 |
Biobank | rs4857855 |
1000 genomes | rs4857855 |
hgdp | rs4857855 |
ensembl | rs4857855 |
geneview | rs4857855 |
scholar | rs4857855 |
rs4857855 | |
pharmgkb | rs4857855 |
gwascentral | rs4857855 |
openSNP | rs4857855 |
23andMe | rs4857855 |
SNPshot | rs4857855 |
SNPdbe | rs4857855 |
MSV3d | rs4857855 |
GWAS Ctlg | rs4857855 |
GMAF | 0.2126 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19198610] |
Trait | Plasma eosinophil count |
Title | Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction |
Risk Allele | T |
P-val | 9E-17 |
Odds Ratio | 9.40 [7.2-11.6] % standard unit increase |