Variant (rsID / SNP)
rs61754141
rs61754141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRIP1. Location: chromosome 17, position 59,820,467. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
BRIP1Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:59820467
- Cytoband
- 17q23.2
- HGVS
- NM_032043.3(BRIP1):c.2286T>C (p.Arg762=)
- Allele change
- Synonymous_R762R
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group J|Neoplasm of ovary|Familial cancer of breast|Fanconi anemia complementation group J|Malignant tumor of breast
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.