NM_001330260.2(SCN8A):c.1999-42A>C AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jun 28, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001552948.3
Allele description [Variation Report for NM_001330260.2(SCN8A):c.1999-42A>C]
NM_001330260.2(SCN8A):c.1999-42A>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Sep 29, 2024