i6008229

A SNP. Its most notable genotype is C;T: lBRCA1 variant of uncertain significance

Gene
None listed
Highest magnitude
3.0Important
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CGoodnormalTypical · 0.0
  2. C;TMost notableBadlBRCA1 variant of uncertain significanceImportant · 3.0

On SNPedia: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Notes

From SNPedia

Notes

For information about causal/pathogenic BRCA1 mutations and what they imply about the odds of developing breast cancer, please see the BRCA1 page and links from that page.

C;T

Although this SNP appears to be rs397509136, a variant of uncertain significance with respect to breast cancer, the correspondence between i6008229 and rs397509136 is not confirmed, due to secrecy policies at 23andMe.

Source and license

Adapted from i6008229 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.