rs397507713(A;G)

BRCA2 variant of uncertain significance

Magnitude
3.6Important
Repute
Bad
On SNPedia
rs397507713(A;G)
Gene
BRCA2

Other genotypes of rs397507713

  1. G;GGoodcommon in clinvarTypical · 0.0
  2. G;TMost notableBadBRCA2 variant considered likely to be pathogenic for breast cancer; see discussion thoughVery important · 5.9

All about rs397507713

Notes

From SNPedia

See discussion at rs397507713; it is not clear if this is a pathogenic mutation according to ClinVar.

Source and license

Adapted from rs397507713(A;G) on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.