rs3733359

A SNP in the GC gene on chromosome 4. Its most notable genotype is G;G: common in complete genomics

Gene
GC
Location
Chr 471,784,057 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
20%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in complete genomicsTypical · 0.063% of people

SNPedia records rs3733359 on the minus strand: (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.

  • AverageG;G 63%
  • European ancestry (Utah)G;G 87%
  • Han Chinese (Beijing)G;G 45%
  • Japanese (Tokyo)G;G 51%
  • Yoruba (Nigeria)G;G 53%
  • African ancestry (Southwest US)G;G 61%
  • Chinese (Denver)G;G 43%
  • Gujarati IndianG;G 86%
  • Luhya (Kenya)G;G 48%
  • Mexican ancestry (Los Angeles)G;G 66%
  • Maasai (Kenya)G;G 55%
  • TuscanG;G 93%

Other GC SNPs

All GC SNPs

Source and license

Adapted from rs3733359 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.