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Variant (rsID / SNP)

rs121908441

KCNE3

rs121908441 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNE3. Location: chromosome 11, position 74,168,313. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

KCNE3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:74168313
Cytoband
11q13.4
HGVS
NM_005472.5(KCNE3):c.296G>A (p.Arg99His)
Allele change
Missense_R99H

Associated conditions / phenotypes

Brugada syndrome 6|Brugada syndrome|Cardiovascular phenotype

Public references

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