rs551660089
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs551660089(A;A) |
| Make rs551660089(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 16 |
| Position | 28894244 |
| Gene | ATP2A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs551660089 |
| dbSNP (classic) | rs551660089 |
| ClinGen | rs551660089 |
| ebi | rs551660089 |
| HLI | rs551660089 |
| Exac | rs551660089 |
| Gnomad | rs551660089 |
| Varsome | rs551660089 |
| LitVar | rs551660089 |
| Map | rs551660089 |
| PheGenI | rs551660089 |
| Biobank | rs551660089 |
| 1000 genomes | rs551660089 |
| hgdp | rs551660089 |
| ensembl | rs551660089 |
| geneview | rs551660089 |
| scholar | rs551660089 |
| rs551660089 | |
| pharmgkb | rs551660089 |
| gwascentral | rs551660089 |
| openSNP | rs551660089 |
| 23andMe | rs551660089 |
| SNPshot | rs551660089 |
| SNPdbe | rs551660089 |
| MSV3d | rs551660089 |
| GWAS Ctlg | rs551660089 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs551660089(A;A) |
| Alt | rs551660089(A;A) |
| Reference | Rs551660089(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | NPIPB8 ATP2A1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000016.9:g.28905565G>A |
| CLNSRC | |
| CLNACC | RCV000424927.1, |
