NM_000447.3(PSEN2):c.69T>C (p.Ala23=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Nov 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001682977.6
Allele description [Variation Report for NM_000447.3(PSEN2):c.69T>C (p.Ala23=)]
NM_000447.3(PSEN2):c.69T>C (p.Ala23=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024