NM_000352.6(ABCC8):c.4722C>G (p.Ala1574=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 31, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002791809.2
Allele description
NM_000352.6(ABCC8):c.4722C>G (p.Ala1574=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024