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Variant (rsID / SNP)

rs138969595

RAD51D

rs138969595 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51D. Location: chromosome 17, position 33,427,976. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

RAD51DConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
17:33427976
Cytoband
17q12
HGVS
NM_002878.4(RAD51D):c.983C>T (p.Thr328Ile)
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4

Public references

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