NM_001159699.2(FHL1):c.537G>C (p.Val179=) AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001502063.7
Allele description [Variation Report for NM_001159699.2(FHL1):c.537G>C (p.Val179=)]
NM_001159699.2(FHL1):c.537G>C (p.Val179=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024