Variant (rsID / SNP)

rs182163363

rs182163363 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNB2. Location: chromosome 10, position 18,787,304. Clinical significance in the table: Benign.

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Reference-table entries

CACNB2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:18787304
Cytoband: 10p12.31
HGVS: NM_201596.3(CACNB2):c.354G>A (p.Ala118=)
Allele change: Synonymous_A118A

Associated conditions / phenotypes

Brugada syndrome 4

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.