rs587777056
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (CCACTTCACATTCAAGAACCT;CCACTTCACATTCAAGAACCT) | 0 | common in clinvar |
| Make rs587777056(-;-) |
| Make rs587777056(-;CATTCAAGAACCTCCACTTCA) |
| Make rs587777056(CATTCAAGAACCTCCACTTCA;CATTCAAGAACCTCCACTTCA) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 56334836 |
| Gene | GNAO1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs587777056 |
| dbSNP (classic) | rs587777056 |
| ClinGen | rs587777056 |
| ebi | rs587777056 |
| HLI | rs587777056 |
| Exac | rs587777056 |
| Gnomad | rs587777056 |
| Varsome | rs587777056 |
| LitVar | rs587777056 |
| Map | rs587777056 |
| PheGenI | rs587777056 |
| Biobank | rs587777056 |
| 1000 genomes | rs587777056 |
| hgdp | rs587777056 |
| ensembl | rs587777056 |
| geneview | rs587777056 |
| scholar | rs587777056 |
| rs587777056 | |
| pharmgkb | rs587777056 |
| gwascentral | rs587777056 |
| openSNP | rs587777056 |
| 23andMe | rs587777056 |
| SNPshot | rs587777056 |
| SNPdbe | rs587777056 |
| MSV3d | rs587777056 |
| GWAS Ctlg | rs587777056 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs587777056(-;-) |
| Alt | rs587777056(-;-) |
| Reference | Rs587777056(CCACTTCACATTCAAGAACCT;CCACTTCACATTCAAGAACCT) |
| Significance | Pathogenic |
| Disease | Early infantile epileptic encephalopathy 17 |
| Variation | info |
| Gene | GNAO1 |
| CLNDBN | Early infantile epileptic encephalopathy 17 |
| Reversed | 0 |
| HGVS | NC_000016.9:g.56368748_56368768del21 |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000056407.27, |
