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rs4646356

From SNPedia

Orientationminus
Stabilizedminus
Make rs4646356(C;C)
Make rs4646356(C;T)
Make rs4646356(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position17567861
GenePEMT
is asnp
is mentioned by
dbSNPrs4646356
ebirs4646356
HLIrs4646356
Exacrs4646356
Varsomers4646356
Maprs4646356
PheGenIrs4646356
hapmaprs4646356
1000 genomesrs4646356
hgdprs4646356
ensemblrs4646356
gopubmedrs4646356
geneviewrs4646356
scholarrs4646356
googlers4646356
pharmgkbrs4646356
gwascentralrs4646356
openSNPrs4646356
23andMers4646356
23andMe allrs4646356
SNP Nexus

SNPshotrs4646356
SNPdbers4646356
MSV3drs4646356
GWAS Ctlgrs4646356
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25074646] Associations of Common Variants in Methionine Metabolism Pathway Genes with Plasma Homocysteine and the Risk of Type 2 Diabetes in Han Chinese