NM_001159699.2(FHL1):c.*7_*8del AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002475494.2
Allele description [Variation Report for NM_001159699.2(FHL1):c.*7_*8del]
NM_001159699.2(FHL1):c.*7_*8del
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024