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rs3885683

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs3885683(A;G)
Make rs3885683(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position83744664
GeneDLG2
is asnp
is mentioned by
dbSNPrs3885683
ebirs3885683
HLIrs3885683
Exacrs3885683
Varsomers3885683
Maprs3885683
PheGenIrs3885683
hapmaprs3885683
1000 genomesrs3885683
hgdprs3885683
ensemblrs3885683
gopubmedrs3885683
geneviewrs3885683
scholarrs3885683
googlers3885683
pharmgkbrs3885683
gwascentralrs3885683
openSNPrs3885683
23andMers3885683
23andMe allrs3885683
SNP Nexus

SNPshotrs3885683
SNPdbers3885683
MSV3drs3885683
GWAS Ctlgrs3885683
GMAF0.06703
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18464913OA-icon.png]
Trait Protein quantitative trait loci
Title A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
Risk Allele
P-val 0.0000079999999999999996
Odds Ratio NR NR

[PMID 18464913OA-icon.png] chemokine ligand 2 (CCL2) / monocyte chemotactic protein-1 (MCP-1) protein levels


GET Evidence
rs3885683
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.03125
summary