NM_000426.4(LAMA2):c.9212-11G>A AND Congenital muscular dystrophy due to partial LAMA2 deficiency
- Germline classification:
- Uncertain significance (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:
- RCV001154397.12
Allele description [Variation Report for NM_000426.4(LAMA2):c.9212-11G>A]
NM_000426.4(LAMA2):c.9212-11G>A
Condition(s)
- Name:
- Congenital muscular dystrophy due to partial LAMA2 deficiency
- Identifiers:
- MedGen: C1842898
-
Ttyh2 tweety family member 2 [Mus musculus]
Ttyh2 tweety family member 2 [Mus musculus]Gene ID:117160Gene
-
117160[uid] AND (alive[prop]) (1)
Gene
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Last Updated: Oct 13, 2024