rs759242559
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs759242559(-;-) |
| Make rs759242559(-;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 1 |
| Position | 229432345 |
| Gene | ACTA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs759242559 |
| dbSNP (classic) | rs759242559 |
| ClinGen | rs759242559 |
| ebi | rs759242559 |
| HLI | rs759242559 |
| Exac | rs759242559 |
| Gnomad | rs759242559 |
| Varsome | rs759242559 |
| LitVar | rs759242559 |
| Map | rs759242559 |
| PheGenI | rs759242559 |
| Biobank | rs759242559 |
| 1000 genomes | rs759242559 |
| hgdp | rs759242559 |
| ensembl | rs759242559 |
| geneview | rs759242559 |
| scholar | rs759242559 |
| rs759242559 | |
| pharmgkb | rs759242559 |
| gwascentral | rs759242559 |
| openSNP | rs759242559 |
| 23andMe | rs759242559 |
| SNPshot | rs759242559 |
| SNPdbe | rs759242559 |
| MSV3d | rs759242559 |
| GWAS Ctlg | rs759242559 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs759242559(-;-) |
| Alt | rs759242559(-;-) |
| Reference | Rs759242559(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ACTA1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.229568092delC |
| CLNSRC | |
| CLNACC | RCV000479633.1, |
