Variant (rsID / SNP)

rs36210419

rs36210419 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ1. Location: chromosome 11, position 2,592,602. Clinical significance in the table: Uncertain significance.

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Reference-table entries

KCNQ1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 11:2592602
Cytoband: 11p15.5
HGVS: NM_000218.3(KCNQ1):c.652A>G (p.Lys218Glu)
Allele change: Missense_K218E

Associated conditions / phenotypes

Torsades de pointes|Long QT syndrome

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.