NM_006227.4(PLTP):c.1360-18C>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003858683.1
Allele description [Variation Report for NM_006227.4(PLTP):c.1360-18C>G]
NM_006227.4(PLTP):c.1360-18C>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024