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rs477992

From SNPedia

Orientationplus
Stabilizedplus
Make rs477992(A;A)
Make rs477992(A;G)
Make rs477992(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position119714953
GenePHGDH
is asnp
is mentioned by
dbSNPrs477992
ebirs477992
HLIrs477992
Exacrs477992
Varsomers477992
Maprs477992
PheGenIrs477992
hapmaprs477992
1000 genomesrs477992
hgdprs477992
ensemblrs477992
gopubmedrs477992
geneviewrs477992
scholarrs477992
googlers477992
pharmgkbrs477992
gwascentralrs477992
openSNPrs477992
23andMers477992
23andMe allrs477992
SNP Nexus

SNPshotrs477992
SNPdbers477992
MSV3drs477992
GWAS Ctlgrs477992
GMAF0.2534
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21886157OA-icon.png]
Trait
Title Human metabolic individuality in biomedical and pharmaceutical research.
Risk Allele A
P-val 3E-14
Odds Ratio 0.0510 None