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Variant (rsID / SNP)

rs370771157

BARD1

rs370771157 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BARD1. Location: chromosome 2, position 215,617,235. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

BARD1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:215617235
Cytoband
2q35
HGVS
NM_000465.4(BARD1):c.1613G>A (p.Ser538Asn)
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Familial cancer of breast

Public references

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