NM_032638.5(GATA2):c.275G>A (p.Ser92Asn) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004366543.1
Allele description [Variation Report for NM_032638.5(GATA2):c.275G>A (p.Ser92Asn)]
NM_032638.5(GATA2):c.275G>A (p.Ser92Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024