rs606231429
From SNPedia
| Merged into | rs397515578 |
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (CTG;CTG) | 0 | common in clinvar |
| Make rs606231429(-;-) |
| Make rs606231429(-;CTG) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 19 |
| Position | 41984930 |
| Gene | ATP1A3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs606231429 |
| dbSNP (classic) | rs606231429 |
| ClinGen | rs606231429 |
| ebi | rs606231429 |
| HLI | rs606231429 |
| Exac | rs606231429 |
| Gnomad | rs606231429 |
| Varsome | rs606231429 |
| LitVar | rs606231429 |
| Map | rs606231429 |
| PheGenI | rs606231429 |
| Biobank | rs606231429 |
| 1000 genomes | rs606231429 |
| hgdp | rs606231429 |
| ensembl | rs606231429 |
| geneview | rs606231429 |
| scholar | rs606231429 |
| rs606231429 | |
| pharmgkb | rs606231429 |
| gwascentral | rs606231429 |
| openSNP | rs606231429 |
| 23andMe | rs606231429 |
| SNPshot | rs606231429 |
| SNPdbe | rs606231429 |
| MSV3d | rs606231429 |
| GWAS Ctlg | rs606231429 |
| Status | Merged into rs397515578 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs606231429(CTG;CTG) |
| Significance | Pathogenic |
| Disease | Dystonia 12 |
| Variation | info |
| Gene | ATP1A3 |
| CLNDBN | Dystonia 12 |
| Reversed | 1 |
| HGVS | NC_000019.9:g.42489082_42489084delCAG |
| CLNSRC | |
| CLNACC | RCV000148307.1, |
