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rs2494250

From SNPedia

Orientationplus
Stabilizedplus
Make rs2494250(C;C)
Make rs2494250(C;G)
Make rs2494250(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position159308461
GeneFCER1A
is asnp
is mentioned by
dbSNPrs2494250
ebirs2494250
HLIrs2494250
Exacrs2494250
Varsomers2494250
Maprs2494250
PheGenIrs2494250
hapmaprs2494250
1000 genomesrs2494250
hgdprs2494250
ensemblrs2494250
gopubmedrs2494250
geneviewrs2494250
scholarrs2494250
googlers2494250
pharmgkbrs2494250
gwascentralrs2494250
openSNPrs2494250
23andMers2494250
23andMe allrs2494250
SNP Nexus

SNPshotrs2494250
SNPdbers2494250
MSV3drs2494250
GWAS Ctlgrs2494250
GMAF0.2062
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS
SNP rs2494250
PubMedID [PMID 17903293OA-icon.png]
Condition Select biomarker traits
Gene FCER1A,OR10J3
Risk Allele
pValue 1.00E-014
OR NA
95% CI


[PMID 17903293OA-icon.png] select biomarker trait being CCL2 (monocyte chemoattractant protein-1, MCP-1) levels



[PMID 17903291OA-icon.png] The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.


[PMID 19474294OA-icon.png] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.


GET Evidence
rs2494250
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.820312
summary