Variant (rsID / SNP)

rs878855292

rs878855292 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,592,969. Clinical significance in the table: Pathogenic.

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Reference-table entries

SCN5APathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 3:38592969
Cytoband: 3p22.2
HGVS: NM_000335.5(SCN5A):c.4891C>T (p.Arg1631Cys)
Allele change: Missense_R1578C

Associated conditions / phenotypes

Brugada syndrome

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.