Variant (rsID / SNP)

rs199473556

rs199473556 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,671,833. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

SCN5APathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 3:38671833
Cytoband: 3p22.2
HGVS: NM_000335.5(SCN5A):c.361C>T (p.Arg121Trp)
Allele change: Missense_R121W

Associated conditions / phenotypes

Brugada syndrome|Brugada syndrome 1|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.