NM_001127644.2(GABRA1):c.269A>G (p.Asp90Gly) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 9, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002774988.2
Allele description [Variation Report for NM_001127644.2(GABRA1):c.269A>G (p.Asp90Gly)]
NM_001127644.2(GABRA1):c.269A>G (p.Asp90Gly)
Condition(s)
- Name:
- Idiopathic generalized epilepsy
- Synonyms:
- EIG; Generalised epilepsy
- Identifiers:
- MONDO: MONDO:0005579; MedGen: C0270850; OMIM: 600669; OMIM: PS600669
Assertion and evidence details
Last Updated: Feb 28, 2024