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Variant (rsID / SNP)

rs767796996

RAD51C

rs767796996 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51C. Location: chromosome 17, position 56,772,550. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

RAD51CPathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
17:56772550
Cytoband
17q22
HGVS
NM_058216.3(RAD51C):c.404G>A (p.Cys135Tyr)
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group O|Hereditary breast ovarian cancer syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.