NM_000815.5(GABRD):c.867G>A (p.Thr289=) AND Idiopathic generalized epilepsy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000550297.9
Allele description [Variation Report for NM_000815.5(GABRD):c.867G>A (p.Thr289=)]
NM_000815.5(GABRD):c.867G>A (p.Thr289=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024