rs11227306

Orientation

plus

Stabilized

plus

Make rs11227306(A;A)

Make rs11227306(A;C)

Make rs11227306(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

65811201

is a	snp
is	mentioned by
dbSNP	rs11227306
dbSNP (classic)	rs11227306
ClinGen	rs11227306
ebi	rs11227306
HLI	rs11227306
Exac	rs11227306
Gnomad	rs11227306
Varsome	rs11227306
LitVar	rs11227306
Map	rs11227306
PheGenI	rs11227306
Biobank	rs11227306
1000 genomes	rs11227306
hgdp	rs11227306
ensembl	rs11227306
geneview	rs11227306
scholar	rs11227306
google	rs11227306
pharmgkb	rs11227306
gwascentral	rs11227306
openSNP	rs11227306
23andMe	rs11227306
SNPshot	rs11227306
SNPdbe	rs11227306
MSV3d	rs11227306
GWAS Ctlg	rs11227306

GMAF

0.3209

Max Magnitude

0

?	(A;A) (A;C) (C;C)	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	A
P-val	2E-7
Odds Ratio	NR NR