Variant (rsID / SNP)

rs73151504

rs73151504 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNA2D1. Location: chromosome 7, position 81,641,500. Clinical significance in the table: Benign.

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Reference-table entries

CACNA2D1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:81641500
Cytoband: 7q21.11
HGVS: NM_000722.4(CACNA2D1):c.1332C>T (p.Val444=)
Allele change: Synonymous_V444V

Associated conditions / phenotypes

Brugada syndrome|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.