NM_000219.6(KCNE1):c.*2194T>C AND Congenital long 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:
- RCV000269432.5
Allele description [Variation Report for NM_000219.6(KCNE1):c.*2194T>C]
NM_000219.6(KCNE1):c.*2194T>C
Condition(s)
-
"Institute of Human Genetics, University of Leipzig Medical Cente... (2)
"Institute of Human Genetics, University of Leipzig Medical Center"[submitter] AND "LOC129994460"[gene]SearchClinVar
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See more...Assertion and evidence details
Last Updated: Apr 9, 2023