rs864309542
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs864309542(C;T) |
| Make rs864309542(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 15 |
| Position | 92978381 |
| Gene | CHD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs864309542 |
| dbSNP (classic) | rs864309542 |
| ClinGen | rs864309542 |
| ebi | rs864309542 |
| HLI | rs864309542 |
| Exac | rs864309542 |
| Gnomad | rs864309542 |
| Varsome | rs864309542 |
| LitVar | rs864309542 |
| Map | rs864309542 |
| PheGenI | rs864309542 |
| Biobank | rs864309542 |
| 1000 genomes | rs864309542 |
| hgdp | rs864309542 |
| ensembl | rs864309542 |
| geneview | rs864309542 |
| scholar | rs864309542 |
| rs864309542 | |
| pharmgkb | rs864309542 |
| gwascentral | rs864309542 |
| openSNP | rs864309542 |
| 23andMe | rs864309542 |
| SNPshot | rs864309542 |
| SNPdbe | rs864309542 |
| MSV3d | rs864309542 |
| GWAS Ctlg | rs864309542 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs864309542(T;T) |
| Alt | rs864309542(T;T) |
| Reference | Rs864309542(C;C) |
| Significance | Pathogenic |
| Disease | Epileptic encephalopathy |
| Variation | info |
| Gene | CHD2 |
| CLNDBN | Epileptic encephalopathy, childhood-onset |
| Reversed | 0 |
| HGVS | NC_000015.9:g.93521611C>T |
| CLNSRC | |
| CLNACC | RCV000202637.1, |
