NM_000335.5(SCN5A):c.3663+10T>C AND not specified
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Oct 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000151782.7
Allele description [Variation Report for NM_000335.5(SCN5A):c.3663+10T>C]
NM_000335.5(SCN5A):c.3663+10T>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 16, 2024