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rs1098774

From SNPedia

Merged intors261097
Orientationminus
Stabilizedplus
Make rs1098774(A;A)
Make rs1098774(A;C)
Make rs1098774(C;C)
ReferenceGRCh38 38.1/142
Chromosome5
Position102123983
is asnp
is mentioned by
dbSNPrs1098774
ebirs1098774
HLIrs1098774
Exacrs1098774
Varsomers1098774
Maprs1098774
PheGenIrs1098774
hapmaprs1098774
1000 genomesrs1098774
hgdprs1098774
ensemblrs1098774
gopubmedrs1098774
geneviewrs1098774
scholarrs1098774
googlers1098774
pharmgkbrs1098774
gwascentralrs1098774
openSNPrs1098774
23andMers1098774
23andMe allrs1098774
SNP Nexus

SNPshotrs1098774
SNPdbers1098774
MSV3drs1098774
GWAS Ctlgrs1098774
StatusMerged into rs261097
Max Magnitude

[PMID 22018726OA-icon.png] Genetic variation in folylpolyglutamate synthase and gamma-glutamyl hydrolase and plasma homocysteine levels in the Singapore Chinese Health Study