NM_014625.4(NPHS2):c.451+9dup AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000958514.7
Allele description [Variation Report for NM_014625.4(NPHS2):c.451+9dup]
NM_014625.4(NPHS2):c.451+9dup
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024