Variant (rsID / SNP)

rs137886232

rs137886232 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51D. Location: chromosome 17, position 33,428,366. Clinical significance in the table: Pathogenic.

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Reference-table entries

RAD51DPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:33428366
Cytoband: 17q12
HGVS: NM_002878.4(RAD51D):c.757C>T (p.Arg253Ter)
Allele change: Silent

Associated conditions / phenotypes

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

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.