NM_003098.3(SNTA1):c.1181G>A (p.Arg394His) AND Congenital long QT syndrome
- Germline classification:
- Uncertain significance (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:
- RCV000374416.5
Allele description [Variation Report for NM_003098.3(SNTA1):c.1181G>A (p.Arg394His)]
NM_003098.3(SNTA1):c.1181G>A (p.Arg394His)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023