NM_006516.4(SLC2A1):c.606C>T (p.Ile202=) AND Epilepsy, idiopathic generalized, susceptibility to, 12
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003446389.1
Allele description [Variation Report for NM_006516.4(SLC2A1):c.606C>T (p.Ile202=)]
NM_006516.4(SLC2A1):c.606C>T (p.Ile202=)
Condition(s)
Assertion and evidence details
Last Updated: Nov 24, 2024