NM_001035.3(RYR2):c.14299-49T>C AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jun 22, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001575998.4
Allele description [Variation Report for NM_001035.3(RYR2):c.14299-49T>C]
NM_001035.3(RYR2):c.14299-49T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024