NM_000349.3(STAR):c.466-11T>C AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002111612.5
Allele description [Variation Report for NM_000349.3(STAR):c.466-11T>C]
NM_000349.3(STAR):c.466-11T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024