NM_001267550.2(TTN):c.98098+12G>A AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 10, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003790189.1
Allele description [Variation Report for NM_001267550.2(TTN):c.98098+12G>A]
NM_001267550.2(TTN):c.98098+12G>A
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024