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rs4857855

From SNPedia

Orientationplus
Stabilizedplus
Make rs4857855(C;C)
Make rs4857855(C;T)
Make rs4857855(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position128541707
is asnp
is mentioned by
dbSNPrs4857855
ebirs4857855
HLIrs4857855
Exacrs4857855
Varsomers4857855
Maprs4857855
PheGenIrs4857855
hapmaprs4857855
1000 genomesrs4857855
hgdprs4857855
ensemblrs4857855
gopubmedrs4857855
geneviewrs4857855
scholarrs4857855
googlers4857855
pharmgkbrs4857855
gwascentralrs4857855
openSNPrs4857855
23andMers4857855
23andMe allrs4857855
SNP Nexus

SNPshotrs4857855
SNPdbers4857855
MSV3drs4857855
GWAS Ctlgrs4857855
GMAF0.2126
Max Magnitude
? (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



GET Evidence
rs4857855
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary