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rs4617146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4617146(C;T)
Make rs4617146(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position63030158
GeneGGH
is asnp
is mentioned by
dbSNPrs4617146
ebirs4617146
HLIrs4617146
Exacrs4617146
Varsomers4617146
Maprs4617146
PheGenIrs4617146
hapmaprs4617146
1000 genomesrs4617146
hgdprs4617146
ensemblrs4617146
gopubmedrs4617146
geneviewrs4617146
scholarrs4617146
googlers4617146
pharmgkbrs4617146
gwascentralrs4617146
openSNPrs4617146
23andMers4617146
23andMe allrs4617146
SNP Nexus

SNPshotrs4617146
SNPdbers4617146
MSV3drs4617146
GWAS Ctlgrs4617146
GMAF0.2686
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 22018726OA-icon.png] Genetic variation in folylpolyglutamate synthase and gamma-glutamyl hydrolase and plasma homocysteine levels in the Singapore Chinese Health Study