NM_174934.4(SCN4B):c.-15G>A AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 29, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000442011.1
Allele description [Variation Report for NM_174934.4(SCN4B):c.-15G>A]
NM_174934.4(SCN4B):c.-15G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 9, 2023