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Variant (rsID / SNP)

rs17215479

KCNQ1

rs17215479 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ1. Location: chromosome 11, position 2,592,593. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

KCNQ1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:2592593
Cytoband
11p15.5
HGVS
NM_000218.3(KCNQ1):c.643G>A (p.Val215Met)
Allele change
Missense_V215M

Associated conditions / phenotypes

Congenital long QT syndrome|Long QT syndrome

Public references

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