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rs10769945

From SNPedia

Orientationplus
Stabilizedplus
Make rs10769945(C;C)
Make rs10769945(C;T)
Make rs10769945(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position1963897
is asnp
is mentioned by
dbSNPrs10769945
ebirs10769945
HLIrs10769945
Exacrs10769945
Varsomers10769945
Maprs10769945
PheGenIrs10769945
hapmaprs10769945
1000 genomesrs10769945
hgdprs10769945
ensemblrs10769945
gopubmedrs10769945
geneviewrs10769945
scholarrs10769945
googlers10769945
pharmgkbrs10769945
gwascentralrs10769945
openSNPrs10769945
23andMers10769945
23andMe allrs10769945
SNP Nexus

SNPshotrs10769945
SNPdbers10769945
MSV3drs10769945
GWAS Ctlgrs10769945
GMAF0.3627
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 T
P-val 5E-7
Odds Ratio NR NR