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Variant (rsID / SNP)

rs397508133

KCNQ1

rs397508133 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ1. Location: chromosome 11, position 2,604,663. The table records no clinical significance for this variant.

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Reference-table entries

KCNQ1Not classified
Variant type
single nucleotide variant
Chromosome / position
11:2604663
Cytoband
11p15.5
HGVS
NM_000218.3(KCNQ1):c.922-2A>C
Allele change
Silent

Associated conditions / phenotypes

Long QT syndrome 1

Public references

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