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rs17261688

From SNPedia

Orientationplus
Stabilizedplus
Make rs17261688(A;A)
Make rs17261688(A;G)
Make rs17261688(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position160107665
is asnp
is mentioned by
dbSNPrs17261688
ebirs17261688
HLIrs17261688
Exacrs17261688
Varsomers17261688
Maprs17261688
PheGenIrs17261688
hapmaprs17261688
1000 genomesrs17261688
hgdprs17261688
ensemblrs17261688
gopubmedrs17261688
geneviewrs17261688
scholarrs17261688
googlers17261688
pharmgkbrs17261688
gwascentralrs17261688
openSNPrs17261688
23andMers17261688
23andMe allrs17261688
SNP Nexus

SNPshotrs17261688
SNPdbers17261688
MSV3drs17261688
GWAS Ctlgrs17261688
GMAF0.06336
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 3E-6
Odds Ratio NR NR