NM_058216.3(RAD51C):c.-13A>G AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jul 7, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000679795.7
Allele description [Variation Report for NM_058216.3(RAD51C):c.-13A>G]
NM_058216.3(RAD51C):c.-13A>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 10, 2024