NM_003383.5(VLDLR):c.2085T>C (p.His695=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 18, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000499465.6
Allele description [Variation Report for NM_003383.5(VLDLR):c.2085T>C (p.His695=)]
NM_003383.5(VLDLR):c.2085T>C (p.His695=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 9, 2023