NM_024426.6(WT1):c.*542G>A AND Meacham syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000298577.6
Allele description [Variation Report for NM_024426.6(WT1):c.*542G>A]
NM_024426.6(WT1):c.*542G>A
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023