NM_000352.6(ABCC8):c.4524G>A (p.Thr1508=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003159614.2
Allele description [Variation Report for NM_000352.6(ABCC8):c.4524G>A (p.Thr1508=)]
NM_000352.6(ABCC8):c.4524G>A (p.Thr1508=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024