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rs12619285

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs12619285(A;G)
Make rs12619285(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position212959321
is asnp
is mentioned by
dbSNPrs12619285
ebirs12619285
HLIrs12619285
Exacrs12619285
Varsomers12619285
Maprs12619285
PheGenIrs12619285
hapmaprs12619285
1000 genomesrs12619285
hgdprs12619285
ensemblrs12619285
gopubmedrs12619285
geneviewrs12619285
scholarrs12619285
googlers12619285
pharmgkbrs12619285
gwascentralrs12619285
openSNPrs12619285
23andMers12619285
23andMe allrs12619285
SNP Nexus

SNPshotrs12619285
SNPdbers12619285
MSV3drs12619285
GWAS Ctlgrs12619285
GMAF0.4059
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19198610]
Trait Plasma eosinophil count
Title Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Risk Allele G
P-val 5E-10
Odds Ratio 6.30 [4.3-8.3] % standard unit increase



[PMID 19860791] Genetic evidence for a role of IL33 in nasal polyposis.


GET Evidence
rs12619285
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.390625
summary



[PMID 23328882] Meta-analyses of four eosinophil related gene variants in coronary heart disease.