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rs9596905

From SNPedia

Orientationplus
Stabilizedplus
Make rs9596905(A;A)
Make rs9596905(A;G)
Make rs9596905(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position54059238
is asnp
is mentioned by
dbSNPrs9596905
ebirs9596905
HLIrs9596905
Exacrs9596905
Varsomers9596905
Maprs9596905
PheGenIrs9596905
hapmaprs9596905
1000 genomesrs9596905
hgdprs9596905
ensemblrs9596905
gopubmedrs9596905
geneviewrs9596905
scholarrs9596905
googlers9596905
pharmgkbrs9596905
gwascentralrs9596905
openSNPrs9596905
23andMers9596905
23andMe allrs9596905
SNP Nexus

SNPshotrs9596905
SNPdbers9596905
MSV3drs9596905
GWAS Ctlgrs9596905
GMAF0.1286
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 A
P-val 2E-6
Odds Ratio NR NR