Variant (rsID / SNP)

rs587782695

rs587782695 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51D. Location: chromosome 17, position 33,433,434. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

RAD51DPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:33433434
Cytoband: 17q12
HGVS: NM_002878.4(RAD51D):c.547C>T (p.Gln183Ter)
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.