NM_000345.4(SNCA):c.*1292_*1296dup AND Parkinson Disease, Dominant
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000374167.5
Allele description [Variation Report for NM_000345.4(SNCA):c.*1292_*1296dup]
NM_000345.4(SNCA):c.*1292_*1296dup
Condition(s)
- Name:
- Parkinson Disease, Dominant
- Identifiers:
- MedGen: CN239359
-
Developmental and epileptic encephalopathy, 60
Developmental and epileptic encephalopathy, 60MedGen
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See more...Assertion and evidence details
Last Updated: Apr 9, 2023