rs869025486
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs869025486(A;A) |
| Make rs869025486(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 3 |
| Position | 46859505 |
| Gene | MYL3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs869025486 |
| dbSNP (classic) | rs869025486 |
| ClinGen | rs869025486 |
| ebi | rs869025486 |
| HLI | rs869025486 |
| Exac | rs869025486 |
| Gnomad | rs869025486 |
| Varsome | rs869025486 |
| LitVar | rs869025486 |
| Map | rs869025486 |
| PheGenI | rs869025486 |
| Biobank | rs869025486 |
| 1000 genomes | rs869025486 |
| hgdp | rs869025486 |
| ensembl | rs869025486 |
| geneview | rs869025486 |
| scholar | rs869025486 |
| rs869025486 | |
| pharmgkb | rs869025486 |
| gwascentral | rs869025486 |
| openSNP | rs869025486 |
| 23andMe | rs869025486 |
| SNPshot | rs869025486 |
| SNPdbe | rs869025486 |
| MSV3d | rs869025486 |
| GWAS Ctlg | rs869025486 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs869025486(A;A) |
| Alt | rs869025486(A;A) |
| Reference | Rs869025486(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Primary familial hypertrophic cardiomyopathy not provided |
| Variation | info |
| Gene | MYL3 |
| CLNDBN | Primary familial hypertrophic cardiomyopathy not provided |
| Reversed | 1 |
| HGVS | NC_000003.11:g.46900995C>T |
| CLNSRC | |
| CLNACC | RCV000208495.1, RCV000426551.1, |
