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Variant (rsID / SNP)

rs587781655

BRIP1

rs587781655 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRIP1. Location: chromosome 17, position 59,885,827. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

BRIP1Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
17:59885827
Cytoband
17q23.2
HGVS
NM_032043.3(BRIP1):c.918+1G>A
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Familial cancer of breast|Fanconi anemia complementation group J|Familial cancer of breast|Fanconi anemia complementation group J

Public references

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