rs9332
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs9332(C;T) |
| Make rs9332(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 7900599 |
| Gene | MTRR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9332 |
| dbSNP (classic) | rs9332 |
| ClinGen | rs9332 |
| ebi | rs9332 |
| HLI | rs9332 |
| Exac | rs9332 |
| Gnomad | rs9332 |
| Varsome | rs9332 |
| LitVar | rs9332 |
| Map | rs9332 |
| PheGenI | rs9332 |
| Biobank | rs9332 |
| 1000 genomes | rs9332 |
| hgdp | rs9332 |
| ensembl | rs9332 |
| geneview | rs9332 |
| scholar | rs9332 |
| rs9332 | |
| pharmgkb | rs9332 |
| gwascentral | rs9332 |
| openSNP | rs9332 |
| 23andMe | rs9332 |
| SNPshot | rs9332 |
| SNPdbe | rs9332 |
| MSV3d | rs9332 |
| GWAS Ctlg | rs9332 |
| GMAF | 0.2231 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19493349
] 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects
[PMID 20445798] Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.
| ClinVar | |
|---|---|
| Risk | rs9332(T;T) |
| Alt | rs9332(T;T) |
| Reference | Rs9332(C;C) |
| 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.7900712G>A |
| CLNSRC | |
| CLNACC | RCV000389294.1, |
