Variant (rsID / SNP)

rs761117662

rs761117662 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,647,507. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SCN5AUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 3:38647507
Cytoband: 3p22.2
HGVS: NM_000335.5(SCN5A):c.1273G>A (p.Ala425Thr)
Allele change: Missense_A425T

Associated conditions / phenotypes

Brugada syndrome|Cardiac arrhythmia

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.