NM_138959.3(VANGL1):c.*1492G>A AND Sacral defect with anterior meningocele
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001099684.4
Allele description [Variation Report for NM_138959.3(VANGL1):c.*1492G>A]
NM_138959.3(VANGL1):c.*1492G>A
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023