Variant (rsID / SNP)

rs17003955

rs17003955 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNE5. Clinical significance in the table: Benign.

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Reference-table entries

KCNE5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq23
HGVS: NM_012282.4(KCNE5):c.97C>T (p.Pro33Ser)
Allele change: Missense_P33S

Associated conditions / phenotypes

Brugada syndrome

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.