rs1770449
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1770449(A;G) |
Make rs1770449(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 236874861 |
Gene | MTR |
is a | snp |
is | mentioned by |
dbSNP | rs1770449 |
dbSNP (classic) | rs1770449 |
ClinGen | rs1770449 |
ebi | rs1770449 |
HLI | rs1770449 |
Exac | rs1770449 |
Gnomad | rs1770449 |
Varsome | rs1770449 |
LitVar | rs1770449 |
Map | rs1770449 |
PheGenI | rs1770449 |
Biobank | rs1770449 |
1000 genomes | rs1770449 |
hgdp | rs1770449 |
ensembl | rs1770449 |
geneview | rs1770449 |
scholar | rs1770449 |
rs1770449 | |
pharmgkb | rs1770449 |
gwascentral | rs1770449 |
openSNP | rs1770449 |
23andMe | rs1770449 |
SNPshot | rs1770449 |
SNPdbe | rs1770449 |
MSV3d | rs1770449 |
GWAS Ctlg | rs1770449 |
GMAF | 0.259 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20180013] Genetic polymorphisms in folate and alcohol metabolism and breast cancer risk: a case-control study in Thai women
[PMID 19493349] 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.
ClinVar | |
---|---|
Risk | rs1770449(G;G) |
Alt | rs1770449(G;G) |
Reference | Rs1770449(A;A) |
Significance | Non-pathogenic |
Disease | not specified Disorders of Intracellular Cobalamin Metabolism |
Variation | info |
Gene | MTR |
CLNDBN | not specified Disorders of Intracellular Cobalamin Metabolism |
Reversed | 1 |
HGVS | NC_000001.10:g.237038161T>C |
CLNSRC | ClinVar GeneDx |
CLNACC | RCV000126867.3, RCV000283784.1, |