rs769215411
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs769215411(A;A) |
| Make rs769215411(A;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 9 |
| Position | 36246163 |
| Gene | GNE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769215411 |
| dbSNP (classic) | rs769215411 |
| ClinGen | rs769215411 |
| ebi | rs769215411 |
| HLI | rs769215411 |
| Exac | rs769215411 |
| Gnomad | rs769215411 |
| Varsome | rs769215411 |
| LitVar | rs769215411 |
| Map | rs769215411 |
| PheGenI | rs769215411 |
| Biobank | rs769215411 |
| 1000 genomes | rs769215411 |
| hgdp | rs769215411 |
| ensembl | rs769215411 |
| geneview | rs769215411 |
| scholar | rs769215411 |
| rs769215411 | |
| pharmgkb | rs769215411 |
| gwascentral | rs769215411 |
| openSNP | rs769215411 |
| 23andMe | rs769215411 |
| SNPshot | rs769215411 |
| SNPdbe | rs769215411 |
| MSV3d | rs769215411 |
| GWAS Ctlg | rs769215411 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs769215411(A;A) |
| Alt | rs769215411(A;A) |
| Reference | Rs769215411(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GNE |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000009.11:g.36246160G>A |
| CLNSRC | |
| CLNACC | RCV000359295.1, |
