NC_000016.9:g.(?_624055)_(2153916_?)dup AND Epilepsy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 27, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001344085.1
Allele description [Variation Report for NC_000016.9:g.(?_624055)_(2153916_?)dup]
NC_000016.9:g.(?_624055)_(2153916_?)dup
Condition(s)
- Name:
- Epilepsy
- Synonyms:
- Seizure Disorders; Seizure disorder
- Identifiers:
- MONDO: MONDO:0005027; MeSH: D004827; MedGen: C0014544
Assertion and evidence details
Last Updated: Jul 15, 2024