NM_004970.3(IGFALS):c.1465G>T (p.Val489Phe) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003251541.2
Allele description [Variation Report for NM_004970.3(IGFALS):c.1465G>T (p.Val489Phe)]
NM_004970.3(IGFALS):c.1465G>T (p.Val489Phe)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024