NM_198904.4(GABRG2):c.987C>A (p.Val329=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001408170.6
Allele description [Variation Report for NM_198904.4(GABRG2):c.987C>A (p.Val329=)]
NM_198904.4(GABRG2):c.987C>A (p.Val329=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024