Variant (rsID / SNP)

rs786205418

rs786205418 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HCN4. Location: chromosome 15, position 73,635,725. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

HCN4Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: Insertion
Chromosome / position: 15:73635725
Cytoband: 15q24.1
HGVS: NM_005477.3(HCN4):c.1209+2_1209+3insGTGA

Associated conditions / phenotypes

Brugada syndrome 8|Ventricular tachycardia

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.