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rs3763558

From SNPedia

Orientationplus
Stabilizedplus
Make rs3763558(A;A)
Make rs3763558(A;C)
Make rs3763558(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position96784503
GeneCPQ
is asnp
is mentioned by
dbSNPrs3763558
ebirs3763558
HLIrs3763558
Exacrs3763558
Varsomers3763558
Maprs3763558
PheGenIrs3763558
hapmaprs3763558
1000 genomesrs3763558
hgdprs3763558
ensemblrs3763558
gopubmedrs3763558
geneviewrs3763558
scholarrs3763558
googlers3763558
pharmgkbrs3763558
gwascentralrs3763558
openSNPrs3763558
23andMers3763558
23andMe allrs3763558
SNP Nexus

SNPshotrs3763558
SNPdbers3763558
MSV3drs3763558
GWAS Ctlgrs3763558
GMAF0.1474
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23725790]
Trait DNA methylation (variation)
Title GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
Risk Allele A
P-val 1E-6
Odds Ratio NR NR