rs5030729
A SNP in the TLR4 gene on chromosome 9. Its most notable genotype is A;A: common in complete genomics
- Gene
- TLR4
- Location
- Chr 9117,712,061 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 4%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). 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.
- AverageA;A 94%
- European ancestry (Utah)A;A 100%
- Han Chinese (Beijing)A;A 100%
- Japanese (Tokyo)A;A 100%
- Yoruba (Nigeria)A;A 76%
Related
Other TLR4 SNPs
- rs4986790G;Gcomplex; numerous associations reportedWorth knowing
- rs4986791T;Tcomplex; see detailsWorth knowing
- rs1554973C;Cincreased risk for chorionic plate inflammationWorth knowing
- rs10759932C;Cincreased risk for chorionic plate inflammationWorth knowing
- rs1927911G;GnormalTypical
- rs5030719G;Gcommon in complete genomicsTypical
- rs10983755G;Gcommon in complete genomicsTypical
- rs11536869A;Acommon genotypeTypical
Source and license
Adapted from rs5030729 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.