rs6063

A SNP in the FGG gene on chromosome 4. Its most notable genotype is T;T.

Gene
FGG
Location
Chr 4154,609,725 (GRCh38)
Highest magnitude
2.0Worth knowing
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
<1%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableNot ratedNo summary available.Worth knowing · 2.00% of people
  2. C;TNot ratedNo summary available.Typical · 0.02% of people
  3. C;CGoodcommonTypical · 0.098% of people

SNPedia records rs6063 on the minus strand: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 7 HapMap populations.

  • AverageT;T 0% C;T 2% C;C 98%
  • European ancestry (Utah)T;T 0% C;T <1% C;C 99%
  • Han Chinese (Beijing)T;T 0% C;T 2% C;C 99%
  • Japanese (Tokyo)T;T 0% C;T <1% C;C 99%
  • Yoruba (Nigeria)T;T 0% C;T 0% C;C 100%
  • Luhya (Kenya)T;T 0% C;T 2% C;C 98%
  • Mexican ancestry (Los Angeles)T;T 0% C;T 2% C;C 98%
  • TuscanT;T 0% C;T 4% C;C 96%

Other FGG SNPs

All FGG SNPs

Notes

From SNPedia

Notes

This is the first snp to experiment with the watson alignment.

Source and license

Adapted from rs6063 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.