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rs10012307

From SNPedia

Orientationplus
Stabilizedplus
Make rs10012307(C;C)
Make rs10012307(C;T)
Make rs10012307(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position136605429
is asnp
is mentioned by
dbSNPrs10012307
dbSNP (classic)rs10012307
ClinGenrs10012307
ebirs10012307
HLIrs10012307
Exacrs10012307
Gnomadrs10012307
Varsomers10012307
LitVarrs10012307
Maprs10012307
PheGenIrs10012307
Biobankrs10012307
1000 genomesrs10012307
hgdprs10012307
ensemblrs10012307
geneviewrs10012307
scholarrs10012307
googlers10012307
pharmgkbrs10012307
gwascentralrs10012307
openSNPrs10012307
23andMers10012307
SNPshotrs10012307
SNPdbers10012307
MSV3drs10012307
GWAS Ctlgrs10012307
GMAF0.2672
Max Magnitude0
? (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 T
P-val 2E-8
Odds Ratio NR NR