Variant (rsID / SNP)

rs137854600

rs137854600 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,592,995. 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: 3:38592995
Cytoband: 3p22.2
HGVS: NM_000335.5(SCN5A):c.4865G>A (p.Arg1622Gln)
Allele change: Missense_R1569Q

Associated conditions / phenotypes

Long QT syndrome 3|Long QT syndrome 3/6, digenic|Congenital long QT syndrome|Brugada 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.