rs397507713(G;G)

Common in clinvar

Magnitude
0.0Typical
Repute
Good
On SNPedia
rs397507713(G;G)
Gene
BRCA2

Other genotypes of rs397507713

  1. A;GBadBRCA2 variant of uncertain significanceImportant · 3.6
  2. G;TMost notableBadBRCA2 variant considered likely to be pathogenic for breast cancer; see discussion thoughVery important · 5.9

All about rs397507713

Source and license

Adapted from rs397507713(G;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.