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rs11227306

From SNPedia

Orientationplus
Stabilizedplus
Make rs11227306(A;A)
Make rs11227306(A;C)
Make rs11227306(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position65811201
is asnp
is mentioned by
dbSNPrs11227306
ebirs11227306
HLIrs11227306
Exacrs11227306
Varsomers11227306
Maprs11227306
PheGenIrs11227306
hapmaprs11227306
1000 genomesrs11227306
hgdprs11227306
ensemblrs11227306
gopubmedrs11227306
geneviewrs11227306
scholarrs11227306
googlers11227306
pharmgkbrs11227306
gwascentralrs11227306
openSNPrs11227306
23andMers11227306
23andMe allrs11227306
SNP Nexus

SNPshotrs11227306
SNPdbers11227306
MSV3drs11227306
GWAS Ctlgrs11227306
GMAF0.3209
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 2E-7
Odds Ratio NR NR