NM_001267550.2(TTN):c.48760+13G>T AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003779455.2
Allele description [Variation Report for NM_001267550.2(TTN):c.48760+13G>T]
NM_001267550.2(TTN):c.48760+13G>T
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024