Variant (rsID / SNP)

rs151153639

rs151153639 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN10A. Location: chromosome 3, position 38,797,287. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SCN10ABenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:38797287
Cytoband: 3p22.2
HGVS: NM_006514.4(SCN10A):c.1453C>T (p.Arg485Cys)
Allele change: Missense_R485C

Associated conditions / phenotypes

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.