NM_000335.5(SCN5A):c.*1820C>G AND Ventricular fibrillation, paroxysmal familial, type 1
- Germline classification:
- Uncertain significance (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:
- RCV001146110.5
Allele description [Variation Report for NM_000335.5(SCN5A):c.*1820C>G]
NM_000335.5(SCN5A):c.*1820C>G
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023