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rs7644516

From SNPedia

Orientationplus
Stabilizedplus
Make rs7644516(A;A)
Make rs7644516(A;G)
Make rs7644516(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position25880794
is asnp
is mentioned by
dbSNPrs7644516
ebirs7644516
HLIrs7644516
Exacrs7644516
Varsomers7644516
Maprs7644516
PheGenIrs7644516
hapmaprs7644516
1000 genomesrs7644516
hgdprs7644516
ensemblrs7644516
gopubmedrs7644516
geneviewrs7644516
scholarrs7644516
googlers7644516
pharmgkbrs7644516
gwascentralrs7644516
openSNPrs7644516
23andMers7644516
23andMe allrs7644516
SNP Nexus

SNPshotrs7644516
SNPdbers7644516
MSV3drs7644516
GWAS Ctlgrs7644516
GMAF0.06841
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 4E-6
Odds Ratio NR NR


[PMID 21281506OA-icon.png] A unified framework for multi-locus association analysis of both common and rare variants.