Variant (rsID / SNP)

rs587780829

rs587780829 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRIP1. Location: chromosome 17, position 59,858,264. Clinical significance in the table: Likely benign.

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Reference-table entries

BRIP1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:59858264
Cytoband: 17q23.2
HGVS: NM_032043.3(BRIP1):c.1731G>A (p.Lys577=)
Allele change: Synonymous_K577K

Associated conditions / phenotypes

Familial cancer of breast|Fanconi anemia complementation group J|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.