Variant (rsID / SNP)

rs876659026

rs876659026 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51D. Location: chromosome 17, position 33,427,968. 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: 17:33427968
Cytoband: 17q12
HGVS: NM_002878.4(RAD51D):c.*4G>A
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome

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.