NM_000218.3(KCNQ1):c.478-8C>T AND Short QT syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000275258.13
Allele description [Variation Report for NM_000218.3(KCNQ1):c.478-8C>T]
NM_000218.3(KCNQ1):c.478-8C>T
Condition(s)
Assertion and evidence details
Last Updated: Apr 20, 2024