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rs1031552

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1031552(C;T)
Make rs1031552(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position63020631
GeneGGH
is asnp
is mentioned by
dbSNPrs1031552
ebirs1031552
HLIrs1031552
Exacrs1031552
Varsomers1031552
Maprs1031552
PheGenIrs1031552
hapmaprs1031552
1000 genomesrs1031552
hgdprs1031552
ensemblrs1031552
gopubmedrs1031552
geneviewrs1031552
scholarrs1031552
googlers1031552
pharmgkbrs1031552
gwascentralrs1031552
openSNPrs1031552
23andMers1031552
23andMe allrs1031552
SNP Nexus

SNPshotrs1031552
SNPdbers1031552
MSV3drs1031552
GWAS Ctlgrs1031552
GMAF0.1818
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


[PMID 17119116OA-icon.png] Gene-nutrient interactions among determinants of folate and one-carbon metabolism on the risk of non-Hodgkin lymphoma: NCI-SEER case-control study.