rs1130459

A SNP in the TF gene on chromosome 3. Its most notable genotype is A;A: common in clinvar

Gene
TF
Location
Chr 3133,746,439 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
38%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in clinvarTypical · 0.09% of people

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 9%
  • European ancestry (Utah)A;A 20%
  • Han Chinese (Beijing)A;A 2%
  • Japanese (Tokyo)A;A 5%
  • Yoruba (Nigeria)A;A 8%

Other TF SNPs

All TF SNPs

Source and license

Adapted from rs1130459 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.