Variant (rsID / SNP)

rs80358062

rs80358062 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,199,652. The table records no clinical significance for this variant.

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Reference-table entries

BRCA1Not classified

Variant type: single nucleotide variant
Chromosome / position: 17:41199652
Cytoband: 17q21.31
HGVS: NM_007294.4(BRCA1):c.5467+8G>T
Allele change: Silent

Associated conditions / phenotypes

Familial cancer of breast|Breast-ovarian cancer, familial, susceptibility to, 1

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.