NM_001320458.2(WNT9B):c.912T>C (p.Ser304=) AND WNT9B-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 7, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003939591.2
Allele description [Variation Report for NM_001320458.2(WNT9B):c.912T>C (p.Ser304=)]
NM_001320458.2(WNT9B):c.912T>C (p.Ser304=)
Condition(s)
- Name:
- WNT9B-related disorder
- Synonyms:
- WNT9B-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Oct 8, 2024