Variant (rsID / SNP)

rs137854609

rs137854609 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,622,661. 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: 3:38622661
Cytoband: 3p22.2
HGVS: NM_000335.5(SCN5A):c.2989G>T (p.Ala997Ser)
Allele change: Missense_A997S

Associated conditions / phenotypes

Long QT syndrome 3|Congenital long QT 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.