NM_000426.4(LAMA2):c.1884+7T>A AND LAMA2-related muscular dystrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002144528.6
Allele description [Variation Report for NM_000426.4(LAMA2):c.1884+7T>A]
NM_000426.4(LAMA2):c.1884+7T>A
Condition(s)
- Name:
- LAMA2-related muscular dystrophy (LAMA2-RD)
- Synonyms:
- Laminin alpha 2-related dystrophy
- Identifiers:
- MONDO: MONDO:0100228; MedGen: C5679788
Assertion and evidence details
Last Updated: Sep 29, 2024