Variant (rsID / SNP)

rs199472758

rs199472758 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ1. Location: chromosome 11, position 2,604,756. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

KCNQ1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:2604756
Cytoband: 11p15.5
HGVS: NM_000218.3(KCNQ1):c.1013C>T (p.Ser338Phe)
Allele change: Missense_S338F

Associated conditions / phenotypes

Long QT syndrome|Congenital 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.