NM_001159699.2(FHL1):c.501G>A (p.Val167=) AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002146260.6
Allele description [Variation Report for NM_001159699.2(FHL1):c.501G>A (p.Val167=)]
NM_001159699.2(FHL1):c.501G>A (p.Val167=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024