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rs4819833

From SNPedia

Orientationplus
Stabilizedplus
Make rs4819833(C;C)
Make rs4819833(C;T)
Make rs4819833(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19703979
is asnp
is mentioned by
dbSNPrs4819833
ebirs4819833
HLIrs4819833
Exacrs4819833
Varsomers4819833
Maprs4819833
PheGenIrs4819833
hapmaprs4819833
1000 genomesrs4819833
hgdprs4819833
ensemblrs4819833
gopubmedrs4819833
geneviewrs4819833
scholarrs4819833
googlers4819833
pharmgkbrs4819833
gwascentralrs4819833
openSNPrs4819833
23andMers4819833
23andMe allrs4819833
SNP Nexus

SNPshotrs4819833
SNPdbers4819833
MSV3drs4819833
GWAS Ctlgrs4819833
GMAF0.3421
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23725790]
Trait DNA methylation (parent-of-origin)
Title GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
Risk Allele C
P-val 6E-8
Odds Ratio NR NR