NM_004646.4(NPHS1):c.1440+2T>C AND Finnish congenital nephrotic syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 19, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000779257.4
Allele description [Variation Report for NM_004646.4(NPHS1):c.1440+2T>C]
NM_004646.4(NPHS1):c.1440+2T>C
Condition(s)
Assertion and evidence details
Last Updated: Jun 10, 2023