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rs10462794

From SNPedia

Orientationplus
Stabilizedplus
Make rs10462794(C;C)
Make rs10462794(C;T)
Make rs10462794(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position4488132
is asnp
is mentioned by
dbSNPrs10462794
ebirs10462794
HLIrs10462794
Exacrs10462794
Varsomers10462794
Maprs10462794
PheGenIrs10462794
hapmaprs10462794
1000 genomesrs10462794
hgdprs10462794
ensemblrs10462794
gopubmedrs10462794
geneviewrs10462794
scholarrs10462794
googlers10462794
pharmgkbrs10462794
gwascentralrs10462794
openSNPrs10462794
23andMers10462794
23andMe allrs10462794
SNP Nexus

SNPshotrs10462794
SNPdbers10462794
MSV3drs10462794
GWAS Ctlgrs10462794
GMAF0.2319
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 5E-6
Odds Ratio NR NR