Variant (rsID / SNP)

rs2270676

rs2270676 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNE3. Location: chromosome 11, position 74,168,411. Clinical significance in the table: Benign.

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Reference-table entries

KCNE3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:74168411
Cytoband: 11q13.4
HGVS: NM_005472.5(KCNE3):c.198T>C (p.Phe66=)
Allele change: Synonymous_F66F

Associated conditions / phenotypes

Cardiovascular phenotype|Brugada syndrome 6

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.