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Variant (rsID / SNP)

rs138362632

KCNQ1

rs138362632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ1. Location: chromosome 11, position 2,591,964. 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
11:2591964
Cytoband
11p15.5
HGVS
NM_000218.3(KCNQ1):c.584G>A (p.Arg195Gln)
Allele change
Missense_R195Q

Associated conditions / phenotypes

Long QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia

Public references

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