NM_001159699.2(FHL1):c.737-13T>C AND not specified
- Germline classification:
- Benign (6 submissions)
- Last evaluated:
- Jul 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000179822.19
Allele description [Variation Report for NM_001159699.2(FHL1):c.737-13T>C]
NM_001159699.2(FHL1):c.737-13T>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 23, 2024