rs4916321
A SNP in the LOC100506023 gene on chromosome 1. Its most notable genotype is G;G: common genotype
- Gene
- LOC100506023
- Location
- Chr 1173,315,060 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 6%
Genotypes
As shown in 23andMe and AncestryDNA files.
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 9 HapMap populations.
- AverageG;G 86%
- European ancestry (Utah)G;G 91%
- Han Chinese (Beijing)G;G 71%
- Japanese (Tokyo)G;G 83%
- Yoruba (Nigeria)G;G 100%
- African ancestry (Southwest US)G;G 93%
- Chinese (Denver)G;G 81%
- Gujarati IndianG;G 93%
- Mexican ancestry (Los Angeles)G;G 69%
- TuscanG;G 90%
Source and license
Adapted from rs4916321 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.