rs3737967
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs3737967(C;T) |
| Make rs3737967(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 1 |
| Position | 11787392 |
| Gene | C1orf167, MTHFR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3737967 |
| dbSNP (classic) | rs3737967 |
| ClinGen | rs3737967 |
| ebi | rs3737967 |
| HLI | rs3737967 |
| Exac | rs3737967 |
| Gnomad | rs3737967 |
| Varsome | rs3737967 |
| LitVar | rs3737967 |
| Map | rs3737967 |
| PheGenI | rs3737967 |
| Biobank | rs3737967 |
| 1000 genomes | rs3737967 |
| hgdp | rs3737967 |
| ensembl | rs3737967 |
| geneview | rs3737967 |
| scholar | rs3737967 |
| rs3737967 | |
| pharmgkb | rs3737967 |
| gwascentral | rs3737967 |
| openSNP | rs3737967 |
| 23andMe | rs3737967 |
| SNPshot | rs3737967 |
| SNPdbe | rs3737967 |
| MSV3d | rs3737967 |
| GWAS Ctlg | rs3737967 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26689687
] Associations of Polymorphisms in MTHFR Gene with the Risk of Age-Related Cataract in Chinese Han Population: A Genotype-Phenotype Analysis.
| ClinVar | |
|---|---|
| Risk | rs3737967(T;T) |
| Alt | rs3737967(T;T) |
| Reference | Rs3737967(C;C) |
| Significance | Probable-non-pathogenic |
| Disease | Neural tube defects |
| Variation | info |
| Gene | MTHFR C1orf167 |
| CLNDBN | Neural tube defects, folate-sensitive |
| Reversed | 1 |
| HGVS | NC_000001.10:g.11847449G>A |
| CLNSRC | |
| CLNACC | RCV000318902.1, |
