NM_000083.3(CLCN1):c.562+5G>C AND Congenital myotonia, autosomal dominant form
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003444482.1
Allele description [Variation Report for NM_000083.3(CLCN1):c.562+5G>C]
NM_000083.3(CLCN1):c.562+5G>C
Condition(s)
Assertion and evidence details
Last Updated: Dec 9, 2023