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Variant (rsID / SNP)

rs150280879

CACNB2

rs150280879 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNB2. Location: chromosome 10, position 18,828,230. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CACNB2Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
10:18828230
Cytoband
10p12.31
HGVS
NM_201596.3(CACNB2):c.1560T>C (p.Pro520=)
Allele change
Synonymous_P520P

Associated conditions / phenotypes

Cardiovascular phenotype|Brugada syndrome 4

Public references

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