rs753198836
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs753198836(A;A) |
| Make rs753198836(A;C) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 19 |
| Position | 1399587 |
| Gene | GAMT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs753198836 |
| dbSNP (classic) | rs753198836 |
| ClinGen | rs753198836 |
| ebi | rs753198836 |
| HLI | rs753198836 |
| Exac | rs753198836 |
| Gnomad | rs753198836 |
| Varsome | rs753198836 |
| LitVar | rs753198836 |
| Map | rs753198836 |
| PheGenI | rs753198836 |
| Biobank | rs753198836 |
| 1000 genomes | rs753198836 |
| hgdp | rs753198836 |
| ensembl | rs753198836 |
| geneview | rs753198836 |
| scholar | rs753198836 |
| rs753198836 | |
| pharmgkb | rs753198836 |
| gwascentral | rs753198836 |
| openSNP | rs753198836 |
| 23andMe | rs753198836 |
| SNPshot | rs753198836 |
| SNPdbe | rs753198836 |
| MSV3d | rs753198836 |
| GWAS Ctlg | rs753198836 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs753198836(A;A) |
| Alt | rs753198836(A;A) |
| Reference | Rs753198836(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GAMT |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000019.9:g.1399586C>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000187565.3, |
