NM_000345.4(SNCA):c.156G>T (p.Val52=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000951877.9
Allele description [Variation Report for NM_000345.4(SNCA):c.156G>T (p.Val52=)]
NM_000345.4(SNCA):c.156G>T (p.Val52=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024