Variant (rsID / SNP)

rs147181577

rs147181577 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HCN4. Location: chromosome 15, position 73,614,847. Clinical significance in the table: Benign.

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Reference-table entries

HCN4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:73614847
Cytoband: 15q24.1
HGVS: NM_005477.3(HCN4):c.3587G>A (p.Arg1196His)
Allele change: Missense_R1196H

Associated conditions / phenotypes

Brugada syndrome 8|Cardiovascular phenotype

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.