Variant (rsID / SNP)

rs1064793326

rs1064793326 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,598,030. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

SCN5ALikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 3:38598030
Cytoband: 3p22.2
HGVS: NM_000335.5(SCN5A):c.4336T>C (p.Tyr1446His)
Allele change: Missense_Y1393H

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.