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Variant (rsID / SNP)

rs62641689

HCN4

rs62641689 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HCN4. Location: chromosome 15, position 73,616,159. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

HCN4Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
15:73616159
Cytoband
15q24.1
HGVS
NM_005477.3(HCN4):c.2275G>A (p.Val759Ile)
Allele change
Missense_V759I

Associated conditions / phenotypes

Sudden cardiac death|Brugada syndrome 8|Sick sinus syndrome 2, autosomal dominant|Cardiovascular phenotype

Public references

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