Variant (rsID / SNP)

rs142735148

rs142735148 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HCN4. Location: chromosome 15, position 73,615,097. 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: 15:73615097
Cytoband: 15q24.1
HGVS: NM_005477.3(HCN4):c.3337A>G (p.Met1113Val)
Allele change: Missense_M1113V

Associated conditions / phenotypes

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

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.