NM_176787.5(PIGN):c.923-19G>A AND Multiple congenital anomalies-hypotonia-seizures syndrome 1
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 18, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003861193.1
Allele description
NM_176787.5(PIGN):c.923-19G>A
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024