NC_000022.11:g.25231905TG[17] AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001786257.2
Allele description [Variation Report for NC_000022.11:g.25231905TG[17]]
NC_000022.11:g.25231905TG[17]
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023