rs10520873
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs10520873(A;G) |
Make rs10520873(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 7901117 |
Gene | MTRR |
is a | snp |
is | mentioned by |
dbSNP | rs10520873 |
dbSNP (classic) | rs10520873 |
ClinGen | rs10520873 |
ebi | rs10520873 |
HLI | rs10520873 |
Exac | rs10520873 |
Gnomad | rs10520873 |
Varsome | rs10520873 |
LitVar | rs10520873 |
Map | rs10520873 |
PheGenI | rs10520873 |
Biobank | rs10520873 |
1000 genomes | rs10520873 |
hgdp | rs10520873 |
ensembl | rs10520873 |
geneview | rs10520873 |
scholar | rs10520873 |
rs10520873 | |
pharmgkb | rs10520873 |
gwascentral | rs10520873 |
openSNP | rs10520873 |
23andMe | rs10520873 |
SNPshot | rs10520873 |
SNPdbe | rs10520873 |
MSV3d | rs10520873 |
GWAS Ctlg | rs10520873 |
GMAF | 0.1997 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20883119] Common polymorphisms in six genes of the methyl group metabolism pathway and obesity in European adolescents
ClinVar | |
---|---|
Risk | rs10520873(G;G) |
Alt | rs10520873(G;G) |
Reference | Rs10520873(A;A) |
Significance | Non-pathogenic |
Disease | Disorders of Intracellular Cobalamin Metabolism |
Variation | info |
Gene | MTRR |
CLNDBN | Disorders of Intracellular Cobalamin Metabolism |
Reversed | 1 |
HGVS | NC_000005.9:g.7901230T>C |
CLNSRC | |
CLNACC | RCV000340298.1, |