NM_198904.4(GABRG2):c.*2095C>G AND Epilepsy, childhood absence 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000401494.5
Allele description [Variation Report for NM_198904.4(GABRG2):c.*2095C>G]
NM_198904.4(GABRG2):c.*2095C>G
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023