rs55776826
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs55776826(C;T) |
| Make rs55776826(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 19 |
| Position | 1399057 |
| Gene | GAMT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs55776826 |
| dbSNP (classic) | rs55776826 |
| ClinGen | rs55776826 |
| ebi | rs55776826 |
| HLI | rs55776826 |
| Exac | rs55776826 |
| Gnomad | rs55776826 |
| Varsome | rs55776826 |
| LitVar | rs55776826 |
| Map | rs55776826 |
| PheGenI | rs55776826 |
| Biobank | rs55776826 |
| 1000 genomes | rs55776826 |
| hgdp | rs55776826 |
| ensembl | rs55776826 |
| geneview | rs55776826 |
| scholar | rs55776826 |
| rs55776826 | |
| pharmgkb | rs55776826 |
| gwascentral | rs55776826 |
| openSNP | rs55776826 |
| 23andMe | rs55776826 |
| SNPshot | rs55776826 |
| SNPdbe | rs55776826 |
| MSV3d | rs55776826 |
| GWAS Ctlg | rs55776826 |
| Max Magnitude | 0 |
rs55776826, also known as c.459+71G>A, is a SNP in the fourth intron of the guanidinoacetate N-methyltransferase GAMT gene on chromosome 19.
rs55776826 been reported as most likely to be a clinically benign polymorphism.[PMID 15108290]
| ClinVar | |
|---|---|
| Risk | rs55776826(T;T) |
| Alt | rs55776826(T;T) |
| Reference | Rs55776826(C;C) |
| Significance | Non-pathogenic |
| Disease | Deficiency of guanidinoacetate methyltransferase |
| Variation | info |
| Gene | GAMT |
| CLNDBN | Deficiency of guanidinoacetate methyltransferase |
| Reversed | 0 |
| HGVS | NC_000019.9:g.1399056C>T |
| CLNSRC | ClinVar GeneReviews |
| CLNACC | RCV000020143.2, |
