NM_000447.3(PSEN2):c.712C>T (p.Leu238Phe) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002490889.8
Allele description [Variation Report for NM_000447.3(PSEN2):c.712C>T (p.Leu238Phe)]
NM_000447.3(PSEN2):c.712C>T (p.Leu238Phe)
Condition(s)
Assertion and evidence details
Last Updated: Oct 20, 2024