Variant (rsID / SNP)

rs144270136

rs144270136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN10A. Location: chromosome 3, position 38,835,234. Clinical significance in the table: Benign.

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Reference-table entries

SCN10ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:38835234
Cytoband: 3p22.2
HGVS: NM_006514.4(SCN10A):c.268C>T (p.Arg90Trp)
Allele change: Missense_R90W

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.