Variant (rsID / SNP)

rs756159737

rs756159737 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,622,784. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SCN5AConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: Microsatellite
Chromosome / position: 3:38622784
Cytoband: 3p22.2
HGVS: NM_000335.5(SCN5A):c.2865_2866del (p.Glu955fs)

Associated conditions / phenotypes

Brugada syndrome|Prolonged QT interval|Sudden cardiac death|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.