rs2070022

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

Gene
FGA
Location
Chr 4154,583,796 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
16%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in complete genomicsTypical · 0.073% of people

SNPedia records rs2070022 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 73%
  • European ancestry (Utah)G;G 73%
  • Han Chinese (Beijing)G;G 80%
  • Japanese (Tokyo)G;G 71%
  • Yoruba (Nigeria)G;G 80%
  • African ancestry (Southwest US)G;G 83%
  • Chinese (Denver)G;G 81%
  • Gujarati IndianG;G 60%
  • Luhya (Kenya)G;G 88%
  • Mexican ancestry (Los Angeles)G;G 51%
  • Maasai (Kenya)G;G 66%
  • TuscanG;G 69%

Notes

From SNPedia

Notes

Identification of type 2 diabetes-associated combination of SNPs using support vector machine. Replication and characterisation of genetic variants in the fibrinogen gene cluster with plasma fibrinogen levels and haematological traits in the Third National Health and Nutrition Examination Survey.

Source and license

Adapted from rs2070022 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.