NM_001171613.2(PREPL):c.-49+1793G>A AND Myasthenic syndrome, congenital, 22
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 15, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001407674.7
Allele description [Variation Report for NM_001171613.2(PREPL):c.-49+1793G>A]
NM_001171613.2(PREPL):c.-49+1793G>A
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024