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Variant (rsID / SNP)

rs373411041

HCN4

rs373411041 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HCN4. Location: chromosome 15, position 73,615,695. 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
15:73615695
Cytoband
15q24.1
HGVS
NM_005477.3(HCN4):c.2739G>A (p.Ala913=)
Allele change
Synonymous_A913A

Associated conditions / phenotypes

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

Public references

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