NM_001040616.3(LINS1):c.2008A>G (p.Lys670Glu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 3, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002460811.2
Allele description [Variation Report for NM_001040616.3(LINS1):c.2008A>G (p.Lys670Glu)]
NM_001040616.3(LINS1):c.2008A>G (p.Lys670Glu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024