NM_001159699.2(FHL1):c.737-7C>T AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002145490.5
Allele description [Variation Report for NM_001159699.2(FHL1):c.737-7C>T]
NM_001159699.2(FHL1):c.737-7C>T
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024