rs755310507
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs755310507(A;A) |
| Make rs755310507(A;C) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 160136307 |
| Gene | ATP1A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs755310507 |
| dbSNP (classic) | rs755310507 |
| ClinGen | rs755310507 |
| ebi | rs755310507 |
| HLI | rs755310507 |
| Exac | rs755310507 |
| Gnomad | rs755310507 |
| Varsome | rs755310507 |
| LitVar | rs755310507 |
| Map | rs755310507 |
| PheGenI | rs755310507 |
| Biobank | rs755310507 |
| 1000 genomes | rs755310507 |
| hgdp | rs755310507 |
| ensembl | rs755310507 |
| geneview | rs755310507 |
| scholar | rs755310507 |
| rs755310507 | |
| pharmgkb | rs755310507 |
| gwascentral | rs755310507 |
| openSNP | rs755310507 |
| 23andMe | rs755310507 |
| SNPshot | rs755310507 |
| SNPdbe | rs755310507 |
| MSV3d | rs755310507 |
| GWAS Ctlg | rs755310507 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs755310507(A;A) rs755310507(T;T) |
| Alt | rs755310507(A;A) rs755310507(T;T) |
| Reference | Rs755310507(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ATP1A2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.160106097C>T |
| CLNSRC | |
| CLNACC | RCV000256148.1, |
