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rs13135284

From SNPedia

Orientationplus
Stabilizedplus
Make rs13135284(C;C)
Make rs13135284(C;T)
Make rs13135284(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position153943598
is asnp
is mentioned by
dbSNPrs13135284
ebirs13135284
HLIrs13135284
Exacrs13135284
Varsomers13135284
Maprs13135284
PheGenIrs13135284
hapmaprs13135284
1000 genomesrs13135284
hgdprs13135284
ensemblrs13135284
gopubmedrs13135284
geneviewrs13135284
scholarrs13135284
googlers13135284
pharmgkbrs13135284
gwascentralrs13135284
openSNPrs13135284
23andMers13135284
23andMe allrs13135284
SNP Nexus

SNPshotrs13135284
SNPdbers13135284
MSV3drs13135284
GWAS Ctlgrs13135284
GMAF0.3434
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23725790]
Trait DNA methylation (parent-of-origin)
Title GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
Risk Allele C
P-val 5E-8
Odds Ratio NR NR