Variant (rsID / SNP)

rs878854562

rs878854562 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51D. Location: chromosome 17, position 33,434,380. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

RAD51DConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 17:33434380
Cytoband: 17q12
HGVS: NM_002878.4(RAD51D):c.345+5A>G
Allele change: Silent

Associated conditions / phenotypes

Breast-ovarian cancer, familial, susceptibility to, 4|Hereditary cancer-predisposing syndrome

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.