NM_000426.4(LAMA2):c.4437-5T>A AND Congenital muscular dystrophy due to partial LAMA2 deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001152674.4
Allele description [Variation Report for NM_000426.4(LAMA2):c.4437-5T>A]
NM_000426.4(LAMA2):c.4437-5T>A
Condition(s)
- Name:
- Congenital muscular dystrophy due to partial LAMA2 deficiency
- Identifiers:
- MedGen: C1842898
Assertion and evidence details
Last Updated: Apr 15, 2024