rs3750861
A SNP in the KLF6 gene on chromosome 10. Its most notable genotype is C;C: common in complete genomics
- Gene
- KLF6
- Location
- Chr 103,782,241 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 6%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). 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.
- AverageC;C 89%
- European ancestry (Utah)C;C 88%
- Han Chinese (Beijing)C;C 88%
- Japanese (Tokyo)C;C 94%
- Yoruba (Nigeria)C;C 98%
- African ancestry (Southwest US)C;C 91%
- Chinese (Denver)C;C 91%
- Gujarati IndianC;C 78%
- Luhya (Kenya)C;C 96%
- Mexican ancestry (Los Angeles)C;C 78%
- Maasai (Kenya)C;C 94%
- TuscanC;C 83%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs10508266 and rs3750861 shows significant association with lung cancer risk rs3750861 affects expression of KLF6 splicing variants in prostate cancer and we found that its rare allele is associated with reduced lung cancer risk
Source and license
Adapted from rs3750861 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.