rs549138385
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs549138385(C;T) |
| Make rs549138385(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 17 |
| Position | 18135747 |
| Gene | MYO15A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs549138385 |
| dbSNP (classic) | rs549138385 |
| ClinGen | rs549138385 |
| ebi | rs549138385 |
| HLI | rs549138385 |
| Exac | rs549138385 |
| Gnomad | rs549138385 |
| Varsome | rs549138385 |
| LitVar | rs549138385 |
| Map | rs549138385 |
| PheGenI | rs549138385 |
| Biobank | rs549138385 |
| 1000 genomes | rs549138385 |
| hgdp | rs549138385 |
| ensembl | rs549138385 |
| geneview | rs549138385 |
| scholar | rs549138385 |
| rs549138385 | |
| pharmgkb | rs549138385 |
| gwascentral | rs549138385 |
| openSNP | rs549138385 |
| 23andMe | rs549138385 |
| SNPshot | rs549138385 |
| SNPdbe | rs549138385 |
| MSV3d | rs549138385 |
| GWAS Ctlg | rs549138385 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs549138385(G;G) rs549138385(T;T) |
| Alt | rs549138385(G;G) rs549138385(T;T) |
| Reference | Rs549138385(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MYO15A |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.18039061C>T |
| CLNSRC | |
| CLNACC | RCV000483838.1, |
