NM_001159699.2(FHL1):c.499G>A (p.Val167Met) AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jan 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000661929.11
Allele description [Variation Report for NM_001159699.2(FHL1):c.499G>A (p.Val167Met)]
NM_001159699.2(FHL1):c.499G>A (p.Val167Met)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024