NM_001082486.2(ACD):c.837G>A (p.Pro279=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002454078.9
Allele description [Variation Report for NM_001082486.2(ACD):c.837G>A (p.Pro279=)]
NM_001082486.2(ACD):c.837G>A (p.Pro279=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Nov 10, 2024