NM_001098426.2(SMARCD2):c.401+20C>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002146309.6
Allele description [Variation Report for NM_001098426.2(SMARCD2):c.401+20C>G]
NM_001098426.2(SMARCD2):c.401+20C>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024