NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro) AND Brugada syndrome 5
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000687916.16
Allele description [Variation Report for NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro)]
NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro)
Condition(s)
Assertion and evidence details
Last Updated: May 19, 2024