NM_000540.3(RYR1):c.1791+14C>T AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 6, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000603754.1
Allele description [Variation Report for NM_000540.3(RYR1):c.1791+14C>T]
NM_000540.3(RYR1):c.1791+14C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: May 19, 2024