Variant (rsID / SNP)

rs397507912

rs397507912 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,929,356. The table records no clinical significance for this variant.

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Reference-table entries

BRCA2Not classified

Variant type: single nucleotide variant
Chromosome / position: 13:32929356
Cytoband: 13q13.1
HGVS: NM_000059.4(BRCA2):c.7366C>G (p.Gln2456Glu)
Allele change: Nonsense_Q2456X

Associated conditions / phenotypes

Familial cancer of breast

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.