Variant (rsID / SNP)
rs199472776
rs199472776 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ1. Location: chromosome 11, position 2,608,860. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
KCNQ1Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:2608860
- Cytoband
- 11p15.5
- HGVS
- NM_000218.3(KCNQ1):c.1189C>T (p.Arg397Trp)
- Allele change
- Missense_R397W
Associated conditions / phenotypes
Congenital long QT syndrome|Long QT syndrome|Long QT syndrome 1|Jervell and Lange-Nielsen syndrome|Short QT syndrome|Familial atrial fibrillation|Wolff-Parkinson-White pattern|Cardiovascular phenotype|Cardiac arrhythmia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.