Variant (rsID / SNP)

rs201641342

rs201641342 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,645,441. 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: 3:38645441
Cytoband: 3p22.2
HGVS: NM_000335.5(SCN5A):c.1652C>T (p.Ala551Val)
Allele change: Missense_A551V

Associated conditions / phenotypes

Brugada syndrome|Brugada syndrome 1|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.