rs997669
A SNP in the CCNE1 gene on chromosome 19. Its most notable genotype is C;C: Very slightly increased (1.18x) increased breast cancer risk
- Gene
- CCNE1
- Location
- Chr 1929,813,576 (GRCh38)
- Highest magnitude
- 1.1Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 22%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TGoodcommon/normal
- C;TNot rated?
- C;CMost notableBadVery slightly increased (1.18x) increased breast cancer risk
SNPedia records rs997669 on the minus strand: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageT;T 71% C;T 25% C;C 4%
- European ancestry (Utah)T;T 39% C;T 50% C;C 12%
- Han Chinese (Beijing)T;T 81% C;T 19% C;C 0%
- Japanese (Tokyo)T;T 85% C;T 14% C;C <1%
- Yoruba (Nigeria)T;T 82% C;T 16% C;C 2%
- African ancestry (Southwest US)T;T 84% C;T 14% C;C 2%
- Chinese (Denver)T;T 84% C;T 16% C;C <1%
- Gujarati IndianT;T 57% C;T 40% C;C 3%
- Luhya (Kenya)T;T 75% C;T 24% C;C 2%
- Mexican ancestry (Los Angeles)T;T 64% C;T 31% C;C 5%
- Maasai (Kenya)T;T 86% C;T 13% C;C 1%
- TuscanT;T 49% C;T 40% C;C 11%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs997669 shows an association with breast cancer in a British study involving ~2300 patients. The odds ratio for the (G;G) vs (A;A) homozygotes is 1.18 (CI: 1.04-1.34, p=0.003).
Source and license
Adapted from rs997669 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.