rs61752062
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs61752062(C;C) |
| Make rs61752062(C;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | X |
| Position | 18647241 |
| Gene | CDKL5, RS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61752062 |
| dbSNP (classic) | rs61752062 |
| ClinGen | rs61752062 |
| ebi | rs61752062 |
| HLI | rs61752062 |
| Exac | rs61752062 |
| Gnomad | rs61752062 |
| Varsome | rs61752062 |
| LitVar | rs61752062 |
| Map | rs61752062 |
| PheGenI | rs61752062 |
| Biobank | rs61752062 |
| 1000 genomes | rs61752062 |
| hgdp | rs61752062 |
| ensembl | rs61752062 |
| geneview | rs61752062 |
| scholar | rs61752062 |
| rs61752062 | |
| pharmgkb | rs61752062 |
| gwascentral | rs61752062 |
| openSNP | rs61752062 |
| 23andMe | rs61752062 |
| SNPshot | rs61752062 |
| SNPdbe | rs61752062 |
| MSV3d | rs61752062 |
| GWAS Ctlg | rs61752062 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs61752062(C;C) |
| Alt | rs61752062(C;C) |
| Reference | Rs61752062(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CDKL5 RS1 |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000023.10:g.18665361C>G |
| CLNSRC | |
| CLNACC | RCV000085261.2, |
