rs4116821

A SNP on chromosome Y. Its most notable genotype is G;G.

Gene
None listed
Location
Chr Y19,910,454 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
26%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableNot ratedNo summary available.Typical · 0.017% 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 4 HapMap populations.

  • AverageG;G 17%
  • European ancestry (Utah)G;G 69%
  • Han Chinese (Beijing)G;G 0%
  • Japanese (Tokyo)G;G 0%
  • Yoruba (Nigeria)G;G 0%

Genosets

Genosets combine several genotypes. Twofold checks them in your report.

Notes

From SNPedia

Notes

In silico and in vitro comparative analysis to select, validate and test SNPs for human identification.

Source and license

Adapted from rs4116821 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.