NM_000237.3(LPL):c.456T>C (p.Asn152=) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jul 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001701240.3
Allele description [Variation Report for NM_000237.3(LPL):c.456T>C (p.Asn152=)]
NM_000237.3(LPL):c.456T>C (p.Asn152=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024