NM_002408.4(MGAT2):c.921A>G (p.Val307=) AND MGAT2-congenital disorder of glycosylation
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001497666.6
Allele description [Variation Report for NM_002408.4(MGAT2):c.921A>G (p.Val307=)]
NM_002408.4(MGAT2):c.921A>G (p.Val307=)
Condition(s)
- Name:
- MGAT2-congenital disorder of glycosylation
- Synonyms:
- CDG IIa; Congenital disorder of glycosylation type 2A; CDG 2A; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0008908; MedGen: C2931008; Orphanet: 79329; OMIM: 212066
Assertion and evidence details
Last Updated: Feb 28, 2024