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Variant (rsID / SNP)

rs376403182

RAD51C

rs376403182 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51C. Location: chromosome 17, position 56,770,011. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

RAD51CConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
17:56770011
Cytoband
17q22
HGVS
NM_058216.3(RAD51C):c.7G>A (p.Gly3Arg)
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group O

Public references

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