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Variant (rsID / SNP)

rs17121819

SCN2B

rs17121819 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN2B. Location: chromosome 11, position 118,039,455. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SCN2BUncertain significance
Clinical significance (as recorded)
Uncertain significance
Variant type
single nucleotide variant
Chromosome / position
11:118039455
Cytoband
11q23.3
HGVS
NM_004588.5(SCN2B):c.82C>T (p.Arg28Trp)
Allele change
Missense_R28W

Associated conditions / phenotypes

Atrial fibrillation, familial, 14

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.