NM_152383.5(DIS3L2):c.53-15G>A AND Perlman syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002098929.5
Allele description [Variation Report for NM_152383.5(DIS3L2):c.53-15G>A]
NM_152383.5(DIS3L2):c.53-15G>A
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024