NM_000218.3(KCNQ1):c.1393+21709T>C AND KCNQ1-related condition
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003893797.1
Allele description [Variation Report for NM_000218.3(KCNQ1):c.1393+21709T>C]
NM_000218.3(KCNQ1):c.1393+21709T>C
Condition(s)
- Name:
- KCNQ1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Mar 16, 2024