Variant (rsID / SNP)

rs77141223

rs77141223 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNB2. Location: chromosome 10, position 18,828,645. Clinical significance in the table: Likely benign.

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Reference-table entries

CACNB2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:18828645
Cytoband: 10p12.31
HGVS: NM_201596.3(CACNB2):c.1975C>T (p.Arg659Cys)
Allele change: Missense_R659C

Associated conditions / phenotypes

Brugada syndrome 4|Cardiovascular phenotype

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.