Variant (rsID / SNP)

rs4796033

rs4796033 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51D. Location: chromosome 17, position 33,433,487. Clinical significance in the table: Benign.

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Reference-table entries

RAD51DBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:33433487
Cytoband: 17q12
HGVS: NM_002878.4(RAD51D):c.494G>A (p.Arg165Gln)
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 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.