Variant (rsID / SNP)

rs794728873

rs794728873 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,616,901. 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: 3:38616901
Cytoband: 3p22.2
HGVS: NM_000335.5(SCN5A):c.3550C>T (p.Gln1184Ter)
Allele change: Nonsense_Q1131X

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.