NM_000335.5(SCN5A):c.3837+6TG[3] AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003657902.2
Allele description [Variation Report for NM_000335.5(SCN5A):c.3837+6TG[3]]
NM_000335.5(SCN5A):c.3837+6TG[3]
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024