rs3823720

A SNP in the GLI3 gene on chromosome 7. Its most notable genotype is G;G: common in clinvar

Gene
GLI3
Location
Chr 741,961,573 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
27%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in clinvarTypical · 0.057% of people

On SNPedia: (G;G). 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.

  • AverageG;G 57%
  • European ancestry (Utah)G;G 52%
  • Han Chinese (Beijing)G;G 34%
  • Japanese (Tokyo)G;G 37%
  • Yoruba (Nigeria)G;G 98%
  • African ancestry (Southwest US)G;G 86%
  • Chinese (Denver)G;G 37%
  • Gujarati IndianG;G 38%
  • Luhya (Kenya)G;G 86%
  • Mexican ancestry (Los Angeles)G;G 48%
  • Maasai (Kenya)G;G 63%
  • TuscanG;G 45%

Other GLI3 SNPs

All GLI3 SNPs

Source and license

Adapted from rs3823720 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.