NM_001166114.2(PNPLA6):c.3816+8T>C AND Hereditary spastic paraplegia 39
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003005141.2
Allele description [Variation Report for NM_001166114.2(PNPLA6):c.3816+8T>C]
NM_001166114.2(PNPLA6):c.3816+8T>C
Condition(s)
Assertion and evidence details
Last Updated: Feb 14, 2024