rs897301304
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 16 |
| Position | 28903043 |
| Gene | ATP2A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs897301304 |
| dbSNP (classic) | rs897301304 |
| ClinGen | rs897301304 |
| ebi | rs897301304 |
| HLI | rs897301304 |
| Exac | rs897301304 |
| Gnomad | rs897301304 |
| Varsome | rs897301304 |
| LitVar | rs897301304 |
| Map | rs897301304 |
| PheGenI | rs897301304 |
| Biobank | rs897301304 |
| 1000 genomes | rs897301304 |
| hgdp | rs897301304 |
| ensembl | rs897301304 |
| geneview | rs897301304 |
| scholar | rs897301304 |
| rs897301304 | |
| pharmgkb | rs897301304 |
| gwascentral | rs897301304 |
| openSNP | rs897301304 |
| 23andMe | rs897301304 |
| SNPshot | rs897301304 |
| SNPdbe | rs897301304 |
| MSV3d | rs897301304 |
| GWAS Ctlg | rs897301304 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs897301304(T;T) |
| Alt | rs897301304(T;T) |
| Reference | Rs897301304(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000016.9:g.28914364C>T |
| CLNSRC | |
| CLNACC | RCV000479735.1, |
