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rs1004689

From SNPedia

Orientationplus
Stabilizedplus
Make rs1004689(G;G)
Make rs1004689(G;T)
Make rs1004689(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position48256185
is asnp
is mentioned by
dbSNPrs1004689
ebirs1004689
HLIrs1004689
Exacrs1004689
Varsomers1004689
Maprs1004689
PheGenIrs1004689
hapmaprs1004689
1000 genomesrs1004689
hgdprs1004689
ensemblrs1004689
gopubmedrs1004689
geneviewrs1004689
scholarrs1004689
googlers1004689
pharmgkbrs1004689
gwascentralrs1004689
openSNPrs1004689
23andMers1004689
23andMe allrs1004689
SNP Nexus

SNPshotrs1004689
SNPdbers1004689
MSV3drs1004689
GWAS Ctlgrs1004689
GMAF0.4945
Max Magnitude
? (G;G) (G;T) (T;T) 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 2E-6
Odds Ratio NR NR