NM_004519.4(KCNQ3):c.*7033T>C AND Benign Neonatal Epilepsy
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000313012.5
Allele description [Variation Report for NM_004519.4(KCNQ3):c.*7033T>C]
NM_004519.4(KCNQ3):c.*7033T>C
Condition(s)
- Name:
- Benign Neonatal Epilepsy
- Identifiers:
- MedGen: C0270851
Assertion and evidence details
Last Updated: Sep 29, 2024