rs28897746(C;T)

BRCA2 variant considered pathogenic for breast cancer

Magnitude
6.0Very important
Repute
Bad
Frequency
<1%Average of 6 populations
On SNPedia
rs28897746(C;T)
Gene
BRCA2

Frequency

Share of people with C;T in each HapMap population.

  • Tuscan2%
  • Han Chinese (Beijing)2%
  • Japanese (Tokyo)<1%
  • Yoruba (Nigeria)<1%
  • African ancestry (Southwest US)0%
  • Maasai (Kenya)0%

Other genotypes of rs28897746

  1. T;TGoodcommon in clinvarTypical · 0.099% of people

All about rs28897746

Notes

From SNPedia

See details via ClinVar link on main SNP/rs# page.

Source and license

Adapted from rs28897746(C;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.