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rs7027203

From SNPedia

Orientationplus
Stabilizedplus
Make rs7027203(A;A)
Make rs7027203(A;C)
Make rs7027203(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position93800281
is asnp
is mentioned by
dbSNPrs7027203
ebirs7027203
HLIrs7027203
Exacrs7027203
Varsomers7027203
Maprs7027203
PheGenIrs7027203
hapmaprs7027203
1000 genomesrs7027203
hgdprs7027203
ensemblrs7027203
gopubmedrs7027203
geneviewrs7027203
scholarrs7027203
googlers7027203
pharmgkbrs7027203
gwascentralrs7027203
openSNPrs7027203
23andMers7027203
23andMe allrs7027203
SNP Nexus

SNPshotrs7027203
SNPdbers7027203
MSV3drs7027203
GWAS Ctlgrs7027203
GMAF0.3067
Max Magnitude
? (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 C
P-val 6E-6
Odds Ratio NR NR