rs4646356
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs4646356(C;C) |
Make rs4646356(C;T) |
Make rs4646356(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 17567861 |
Gene | PEMT |
is a | snp |
is | mentioned by |
dbSNP | rs4646356 |
dbSNP (classic) | rs4646356 |
ClinGen | rs4646356 |
ebi | rs4646356 |
HLI | rs4646356 |
Exac | rs4646356 |
Gnomad | rs4646356 |
Varsome | rs4646356 |
LitVar | rs4646356 |
Map | rs4646356 |
PheGenI | rs4646356 |
Biobank | rs4646356 |
1000 genomes | rs4646356 |
hgdp | rs4646356 |
ensembl | rs4646356 |
geneview | rs4646356 |
scholar | rs4646356 |
rs4646356 | |
pharmgkb | rs4646356 |
gwascentral | rs4646356 |
openSNP | rs4646356 |
23andMe | rs4646356 |
SNPshot | rs4646356 |
SNPdbe | rs4646356 |
MSV3d | rs4646356 |
GWAS Ctlg | rs4646356 |
Max Magnitude | 0 |
? | (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