Variant (rsID / SNP)
rs201682200
rs201682200 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ1. Location: chromosome 11, position 2,549,151. 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
- 11:2549151
- Cytoband
- 11p15.5
- HGVS
- NM_000218.3(KCNQ1):c.387-7C>T
- Allele change
- Silent
Associated conditions / phenotypes
Jervell and Lange-Nielsen syndrome 1|Atrial fibrillation, familial, 3|Congenital long QT syndrome|Long QT syndrome|Short QT syndrome type 2|Long QT syndrome 1|Cardiac arrhythmia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.