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Variant (rsID / SNP)

rs41313031

SCN5A

rs41313031 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,603,947. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SCN5ABenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
3:38603947
Cytoband
3p22.2
HGVS
NM_000335.5(SCN5A):c.3919C>T (p.Leu1307Phe)
Allele change
Missense_L1254F

Associated conditions / phenotypes

Brugada syndrome, lidocaine-induced|Cardiovascular phenotype|Brugada syndrome 1|Brugada syndrome|Cardiac arrhythmia

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.