Variant (rsID / SNP)

rs74120235

rs74120235 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNB2. Location: chromosome 10, position 18,439,808. 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: 10:18439808
Cytoband: 10p12.33
HGVS: NM_201596.3(CACNB2):c.121-4T>G
Allele change: Silent

Associated conditions / phenotypes

Short QT Syndrome 5

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.