Variant (rsID / SNP)

rs199472710

rs199472710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ1. Location: chromosome 11, position 2,593,263. Clinical significance in the table: Pathogenic.

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Reference-table entries

KCNQ1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:2593263
Cytoband: 11p15.5
HGVS: NM_000218.3(KCNQ1):c.704T>A (p.Ile235Asn)
Allele change: Missense_I235N

Associated conditions / phenotypes

Congenital long QT syndrome|Long QT syndrome|Cardiac arrhythmia

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.