rs786205487
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs786205487(A;T) |
| Make rs786205487(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 14 |
| Position | 50620724 |
| Gene | ATL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs786205487 |
| dbSNP (classic) | rs786205487 |
| ClinGen | rs786205487 |
| ebi | rs786205487 |
| HLI | rs786205487 |
| Exac | rs786205487 |
| Gnomad | rs786205487 |
| Varsome | rs786205487 |
| LitVar | rs786205487 |
| Map | rs786205487 |
| PheGenI | rs786205487 |
| Biobank | rs786205487 |
| 1000 genomes | rs786205487 |
| hgdp | rs786205487 |
| ensembl | rs786205487 |
| geneview | rs786205487 |
| scholar | rs786205487 |
| rs786205487 | |
| pharmgkb | rs786205487 |
| gwascentral | rs786205487 |
| openSNP | rs786205487 |
| 23andMe | rs786205487 |
| SNPshot | rs786205487 |
| SNPdbe | rs786205487 |
| MSV3d | rs786205487 |
| GWAS Ctlg | rs786205487 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs786205487(T;T) |
| Alt | rs786205487(T;T) |
| Reference | Rs786205487(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ATL1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000014.8:g.51087442A>T |
| CLNSRC | |
| CLNACC | RCV000171222.1, |
