rs4129009
A SNP in the TLR10 gene on chromosome 4. Its most notable genotype is T;T: common in complete genomics
- Gene
- TLR10
- Location
- Chr 438,773,268 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- FamilyTreeDNA
- Minor allele frequency
- 19%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs4129009 on the minus strand: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageT;T 62%
- European ancestry (Utah)T;T 65%
- Han Chinese (Beijing)T;T 38%
- Japanese (Tokyo)T;T 23%
- African ancestry (Southwest US)T;T 89%
- Chinese (Denver)T;T 47%
- Gujarati IndianT;T 68%
- Mexican ancestry (Los Angeles)T;T 83%
- Maasai (Kenya)T;T 95%
- TuscanT;T 48%
Related
Notes
From SNPedia
Notes
Toll-like receptor signaling pathway variants and prostate cancer mortality. Genetic variants and prostate cancer risk: candidate replication and exploration of viral restriction genes. Sequence variants in the TLR4 and TLR6-1-10 genes and prostate cancer risk. Results based on pooled analysis from three independent studies. Association between toll-like receptor 10 (TLR10) gene polymorphisms and childhood IgA nephropathy. Association of polymorphisms in TLR genes and in genes of the Toll-like receptor signaling pathway with cancer risk. Association between C13ORF31, NOD2, RIPK2 and TLR10 polymorphisms and urothelial bladder cancer.
Source and license
Adapted from rs4129009 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.