Variant (rsID / SNP)

rs759292615

rs759292615 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51C. Location: chromosome 17, position 56,809,884. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

RAD51CLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:56809884
Cytoband: 17q22
HGVS: NM_058216.3(RAD51C):c.1005C>A (p.Cys335Ter)
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group O

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.