| Individual ID | 28503910.225 |
|---|---|
| Pubmed ID | 28503910 |
| Whose mosaic mutation | Father |
| Phenotypic Category | 2 |
| Number of affected children | 1 |
| Disease | Autism Spectrum Disorders(view all the variants in this disease) |
| OMIM ID | 209850 |
Found 1 variant in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 30001 | 23416 | KCNH3 | 12 | 49937116 | 49937116 | Autism Spectrum Disorders | PASM |