rs3776455
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3776455(A;A) |
Make rs3776455(A;G) |
Make rs3776455(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 7896398 |
Gene | MTRR |
is a | snp |
is | mentioned by |
dbSNP | rs3776455 |
dbSNP (classic) | rs3776455 |
ClinGen | rs3776455 |
ebi | rs3776455 |
HLI | rs3776455 |
Exac | rs3776455 |
Gnomad | rs3776455 |
Varsome | rs3776455 |
LitVar | rs3776455 |
Map | rs3776455 |
PheGenI | rs3776455 |
Biobank | rs3776455 |
1000 genomes | rs3776455 |
hgdp | rs3776455 |
ensembl | rs3776455 |
geneview | rs3776455 |
scholar | rs3776455 |
rs3776455 | |
pharmgkb | rs3776455 |
gwascentral | rs3776455 |
openSNP | rs3776455 |
23andMe | rs3776455 |
SNPshot | rs3776455 |
SNPdbe | rs3776455 |
MSV3d | rs3776455 |
GWAS Ctlg | rs3776455 |
GMAF | 0.4871 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23940529] Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by bayesian relevance and effect size analysis
[PMID 19493349] 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.