Variant (rsID / SNP)

rs587782818

rs587782818 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51C. Location: chromosome 17, position 56,780,686. Clinical significance in the table: Pathogenic.

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Reference-table entries

RAD51CPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:56780686
Cytoband: 17q22
HGVS: NM_058216.3(RAD51C):c.701C>G (p.Ser234Ter)
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group O|Breast-ovarian cancer, familial, susceptibility to, 3|Fanconi anemia complementation group O|Malignant tumor of breast

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.