NM_005430.4(WNT1):c.358+13del AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002139243.5
Allele description [Variation Report for NM_005430.4(WNT1):c.358+13del]
NM_005430.4(WNT1):c.358+13del
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024