NM_001082486.1(ACD):c.66G>A (p.Ala22=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 14, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002367146.9
Allele description [Variation Report for NM_001082486.1(ACD):c.66G>A (p.Ala22=)]
NM_001082486.1(ACD):c.66G>A (p.Ala22=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Jun 2, 2024