rs2227692
A SNP in the SERPINE1 gene on chromosome 7. Its most notable genotype is C;T: 1.6x higher risk for diffuse gastric cancer
- Gene
- SERPINE1
- Location
- Chr 7101,135,963 (GRCh38)
- Highest magnitude
- 1.6Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 21%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in complete genomics
- C;TMost notableBad1.6x higher risk for diffuse gastric cancer
- T;TBad1.6x higher risk for diffuse gastric cancer
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 62% C;T 34% T;T 4%
- European ancestry (Utah)C;C 86% C;T 14% T;T 0%
- Han Chinese (Beijing)C;C 47% C;T 47% T;T 7%
- Japanese (Tokyo)C;C 42% C;T 53% T;T 4%
- Yoruba (Nigeria)C;C 74% C;T 22% T;T 3%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs2227692, also known as c.1162+162C>T, is a SNP in the SERPINE1 gene. A study of 612 Korean patients with gastric cancer concluded that the rs2227692 C/T and T/T genotypes had 1.6x greater risk for diffuse gastric cancer than the C/C genotype (p = .00084).
C;T
see discussion at rs2227692
T;T
see discussion at rs2227692
Source and license
Adapted from rs2227692 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.