NM_198904.4(GABRG2):c.768C>T (p.Ser256=) AND Epilepsy, childhood absence 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000309729.6
Allele description [Variation Report for NM_198904.4(GABRG2):c.768C>T (p.Ser256=)]
NM_198904.4(GABRG2):c.768C>T (p.Ser256=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 20, 2024