Variant (rsID / SNP)

rs200546024

rs200546024 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HCN4. Location: chromosome 15, position 73,615,912. Clinical significance in the table: Likely benign.

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Reference-table entries

HCN4Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:73615912
Cytoband: 15q24.1
HGVS: NM_005477.3(HCN4):c.2522C>T (p.Ser841Leu)
Allele change: Missense_S841L

Associated conditions / phenotypes

Brugada syndrome 8

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.