rs13306561
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs13306561(C;C) |
| Make rs13306561(C;T) |
| Make rs13306561(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 11805747 |
| Gene | CLCN6, MTHFR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13306561 |
| dbSNP (classic) | rs13306561 |
| ClinGen | rs13306561 |
| ebi | rs13306561 |
| HLI | rs13306561 |
| Exac | rs13306561 |
| Gnomad | rs13306561 |
| Varsome | rs13306561 |
| LitVar | rs13306561 |
| Map | rs13306561 |
| PheGenI | rs13306561 |
| Biobank | rs13306561 |
| 1000 genomes | rs13306561 |
| hgdp | rs13306561 |
| ensembl | rs13306561 |
| geneview | rs13306561 |
| scholar | rs13306561 |
| rs13306561 | |
| pharmgkb | rs13306561 |
| gwascentral | rs13306561 |
| openSNP | rs13306561 |
| 23andMe | rs13306561 |
| SNPshot | rs13306561 |
| SNPdbe | rs13306561 |
| MSV3d | rs13306561 |
| GWAS Ctlg | rs13306561 |
| GMAF | 0.1382 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22241680
] Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningocele
[PMID 32117640] Single nucleotide polymorphism of MTHFR rs1801133 associated with elevated Hcy levels affects susceptibility to cerebral small vessel disease.
