NM_001159699.2(FHL1):c.736+8A>G AND FHL1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003962783.2
Allele description [Variation Report for NM_001159699.2(FHL1):c.736+8A>G]
NM_001159699.2(FHL1):c.736+8A>G
Condition(s)
- Name:
- FHL1-related disorder
- Synonyms:
- FHL1-related condition; FHL1-related disorders
- Identifiers:
Assertion and evidence details
Last Updated: Nov 3, 2024