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rs4128725

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs4128725(C;C)
Make rs4128725(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position159436169
GeneOR10J1
is asnp
is mentioned by
dbSNPrs4128725
ebirs4128725
HLIrs4128725
Exacrs4128725
Varsomers4128725
Maprs4128725
PheGenIrs4128725
hapmaprs4128725
1000 genomesrs4128725
hgdprs4128725
ensemblrs4128725
gopubmedrs4128725
geneviewrs4128725
scholarrs4128725
googlers4128725
pharmgkbrs4128725
gwascentralrs4128725
openSNPrs4128725
23andMers4128725
23andMe allrs4128725
SNP Nexus

SNPshotrs4128725
SNPdbers4128725
MSV3drs4128725
GWAS Ctlgrs4128725
GMAF0.1341
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 17903293OA-icon.png] select biomarker trait being CCL2 (monocyte chemoattractant protein-1, MCP-1) levels
GWAS
SNP rs4128725
PubMedID [PMID 17903293OA-icon.png]
Condition Select biomarker traits
Gene OR10J1
Risk Allele
pValue 4.00E-012
OR NA
95% CI



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


GET Evidence
rs4128725
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.101562
summary