NM_000033.4(ABCD1):c.1317G>A (p.Glu439=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 6, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002384682.2
Allele description [Variation Report for NM_000033.4(ABCD1):c.1317G>A (p.Glu439=)]
NM_000033.4(ABCD1):c.1317G>A (p.Glu439=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 8, 2024