NM_001159699.2(FHL1):c.737-10T>C AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001452374.14
Allele description [Variation Report for NM_001159699.2(FHL1):c.737-10T>C]
NM_001159699.2(FHL1):c.737-10T>C
Condition(s)
Assertion and evidence details
Last Updated: Jun 29, 2024