rs3768160
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs3768160(C;C) |
| Make rs3768160(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 236899132 |
| Gene | MTR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3768160 |
| dbSNP (classic) | rs3768160 |
| ClinGen | rs3768160 |
| ebi | rs3768160 |
| HLI | rs3768160 |
| Exac | rs3768160 |
| Gnomad | rs3768160 |
| Varsome | rs3768160 |
| LitVar | rs3768160 |
| Map | rs3768160 |
| PheGenI | rs3768160 |
| Biobank | rs3768160 |
| 1000 genomes | rs3768160 |
| hgdp | rs3768160 |
| ensembl | rs3768160 |
| geneview | rs3768160 |
| scholar | rs3768160 |
| rs3768160 | |
| pharmgkb | rs3768160 |
| gwascentral | rs3768160 |
| openSNP | rs3768160 |
| 23andMe | rs3768160 |
| SNPshot | rs3768160 |
| SNPdbe | rs3768160 |
| MSV3d | rs3768160 |
| GWAS Ctlg | rs3768160 |
| GMAF | 0.08999 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20737570] Genetic variants in one-carbon metabolism-related genes contribute to NSCLC prognosis in a Chinese population
| ClinVar | |
|---|---|
| Risk | rs3768160(C;C) |
| Alt | rs3768160(C;C) |
| Reference | Rs3768160(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | Disorders of Intracellular Cobalamin Metabolism |
| Variation | info |
| Gene | MTR |
| CLNDBN | Disorders of Intracellular Cobalamin Metabolism |
| Reversed | 0 |
| HGVS | NC_000001.10:g.237062432T>C |
| CLNSRC | |
| CLNACC | RCV000331743.1, |
