NM_000527.5(LDLR):c.269A>G (p.Asp90Gly) AND Homozygous familial hypercholesterolemia
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Oct 23, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000844733.5
Allele description [Variation Report for NM_000527.5(LDLR):c.269A>G (p.Asp90Gly)]
NM_000527.5(LDLR):c.269A>G (p.Asp90Gly)
Condition(s)
- Name:
- Homozygous familial hypercholesterolemia
- Synonyms:
- Familial hypercholesterolemia - homozygous
- Identifiers:
- MONDO: MONDO:0018328; MedGen: C0342881
Assertion and evidence details
Last Updated: Jun 23, 2024