NM_000218.3(KCNQ1):c.1393+21582A>G AND KCNQ1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004532043.1
Allele description [Variation Report for NM_000218.3(KCNQ1):c.1393+21582A>G]
NM_000218.3(KCNQ1):c.1393+21582A>G
Condition(s)
- Name:
- KCNQ1-related disorder
- Synonyms:
- KCNQ1-Related Disorders; KCNQ1-related condition
- Identifiers:
- MedGen: CN239322
Assertion and evidence details
Last Updated: Jun 9, 2024