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Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden

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1. ClingenBaseline 23 Oct 2026
  
  in Baseline Annotations
  
  Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden
  
  PMID: 28532774
  
  Gene: KCNQ1
  
  HGNC: 6294
  
  General ClinGen Gene:KCNQ1 HGNC:6294 inferred_gene_hgnc:6294 inferred_gene_source:hgnc_tag Retina GCEP
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Gene:KCNQ1

inferred_gene_hgnc:6294

General

Retina GCEP

HGNC:6294

inferred_gene_source:hgnc_tag

ClinGen

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ClingenBaseline

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academic.oup.com/europace/article/14/12/1799/526510