Have questions? Visit https://www.reddit.com/r/SNPedia

rs3858526

From SNPedia

Orientationminus
Stabilizedminus
Make rs3858526(G;G)
Make rs3858526(G;T)
Make rs3858526(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5938527
is asnp
is mentioned by
dbSNPrs3858526
dbSNP (old)rs3858526
ClinGenrs3858526
ebirs3858526
HLIrs3858526
Exacrs3858526
Varsomers3858526
Maprs3858526
PheGenIrs3858526
Biobankrs3858526
1000 genomesrs3858526
hgdprs3858526
ensemblrs3858526
gopubmedrs3858526
geneviewrs3858526
scholarrs3858526
googlers3858526
pharmgkbrs3858526
gwascentralrs3858526
openSNPrs3858526
23andMers3858526
23andMe allrs3858526
SNP Nexus

SNPshotrs3858526
SNPdbers3858526
MSV3drs3858526
GWAS Ctlgrs3858526
GMAF0.2713
Max Magnitude
? (G;G) (G;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 3E-6
Odds Ratio NR NR