NM_001909.5(CTSD):c.972+9C>T AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 22, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000733126.6
Allele description [Variation Report for NM_001909.5(CTSD):c.972+9C>T]
NM_001909.5(CTSD):c.972+9C>T
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024