Variant (rsID / SNP)

rs794728565

rs794728565 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ1. Location: chromosome 11, position 2,549,173. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

KCNQ1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: Deletion
Chromosome / position: 11:2549173
Cytoband: 11p15.5
HGVS: NM_000218.3(KCNQ1):c.403del (p.Val135fs)

Associated conditions / phenotypes

Congenital long QT syndrome|Jervell and Lange-Nielsen 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.