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rs4304977

From SNPedia

Orientationplus
Stabilizedplus
Make rs4304977(A;A)
Make rs4304977(A;G)
Make rs4304977(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position92263061
is asnp
is mentioned by
dbSNPrs4304977
dbSNP (classic)rs4304977
ClinGenrs4304977
ebirs4304977
HLIrs4304977
Exacrs4304977
Gnomadrs4304977
Varsomers4304977
LitVarrs4304977
Maprs4304977
PheGenIrs4304977
Biobankrs4304977
1000 genomesrs4304977
hgdprs4304977
ensemblrs4304977
geneviewrs4304977
scholarrs4304977
googlers4304977
pharmgkbrs4304977
gwascentralrs4304977
openSNPrs4304977
23andMers4304977
SNPshotrs4304977
SNPdbers4304977
MSV3drs4304977
GWAS Ctlgrs4304977
GMAF0.4513
Max Magnitude0
? (A;A) (A;G) (G;G) 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 5E-6
Odds Ratio NR NR