NM_001371596.2(MFSD8):c.1320A>G (p.Leu440=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002379299.9
Allele description [Variation Report for NM_001371596.2(MFSD8):c.1320A>G (p.Leu440=)]
NM_001371596.2(MFSD8):c.1320A>G (p.Leu440=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Nov 10, 2024