rs10462794

Orientation

plus

Stabilized

plus

Make rs10462794(C;C)

Make rs10462794(C;T)

Make rs10462794(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

4488132

is a	snp
is	mentioned by
dbSNP	rs10462794
dbSNP (classic)	rs10462794
ClinGen	rs10462794
ebi	rs10462794
HLI	rs10462794
Exac	rs10462794
Gnomad	rs10462794
Varsome	rs10462794
LitVar	rs10462794
Map	rs10462794
PheGenI	rs10462794
Biobank	rs10462794
1000 genomes	rs10462794
hgdp	rs10462794
ensembl	rs10462794
geneview	rs10462794
scholar	rs10462794
google	rs10462794
pharmgkb	rs10462794
gwascentral	rs10462794
openSNP	rs10462794
23andMe	rs10462794
SNPshot	rs10462794
SNPdbe	rs10462794
MSV3d	rs10462794
GWAS Ctlg	rs10462794

GMAF

0.2319

Max Magnitude

0

?	(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