rs12184413
A SNP in the MMP7 gene on chromosome 11. Its most notable genotype is C;C: normal
- Gene
- MMP7
- Location
- Chr 11102,518,857 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 14%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageC;C 72% C;T 26% T;T 2%
- European ancestry (Utah)C;C 81% C;T 17% T;T 2%
- Han Chinese (Beijing)C;C 46% C;T 46% T;T 7%
- Japanese (Tokyo)C;C 61% C;T 39% T;T 0%
- Yoruba (Nigeria)C;C 100% C;T 0% T;T 0%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs12184413(T;T) was associated with reduced risk for breast cancer, with an odds ratio of 0.7 (CI: 0.6-0.9), based on a study ultimately totaling over 3,000 cases (and an equal number of controls). Genetic polymorphisms in the MMP-7 gene and breast cancer survival. No association between matrix metalloproteinase (MMP)-1, MMP-3, and MMP-7 SNPs and endometrial cancer risk.
Source and license
Adapted from rs12184413 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.