rs28897686(C;T)

Benign BRCA1 variant

Magnitude
1.0Minor
Repute
Good
Frequency
0%Average of 1 populations
On SNPedia
rs28897686(A;G)Minus strand
Gene
BRCA1

Frequency

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

  • Japanese (Tokyo)0%

Other genotypes of rs28897686

  1. C;CGoodcommon in clinvarTypical · 0.01% of people
  2. A;CMost notableBadBRCA1 pathogenic mutation associated with breast cancerVery important · 6.099% of people

All about rs28897686

Notes

From SNPedia

see discussion at rs28897686

Source and license

Adapted from rs28897686(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.