NM_001082486.2(ACD):c.99+18G>A AND not provided
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004710397.1
Allele description [Variation Report for NM_001082486.2(ACD):c.99+18G>A]
NM_001082486.2(ACD):c.99+18G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024