NM_000157.4(GBA1):c.1343A>T (p.Asp448Val) AND Gaucher disease type I
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Dec 21, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000411499.2
Allele description [Variation Report for NM_000157.4(GBA1):c.1343A>T (p.Asp448Val)]
NM_000157.4(GBA1):c.1343A>T (p.Asp448Val)
Condition(s)
- Name:
- Gaucher disease type I (GD1)
- Synonyms:
- GBA DEFICIENCY; GD I; Gaucher's disease, type 1; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009265; MedGen: C1961835; Orphanet: 355; Orphanet: 77259; OMIM: 230800
Assertion and evidence details
Last Updated: Jul 29, 2023