Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs147241704

RAD51C

rs147241704 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51C. Location: chromosome 17, position 56,787,304. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

RAD51CConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
17:56787304
Cytoband
17q22
HGVS
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)
Allele change
Silent

Associated conditions / phenotypes

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

Public references

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