rs16964476
A SNP in the SCG3 gene on chromosome 15. Its most notable genotype is A;A: common in complete genomics
- Gene
- SCG3
- Location
- Chr 1551,682,027 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 7%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). 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.
- AverageA;A 80%
- European ancestry (Utah)A;A 100%
- Han Chinese (Beijing)A;A 87%
- Japanese (Tokyo)A;A 73%
- Yoruba (Nigeria)A;A 62%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs16964465 rs16964476 may influence the risk of obesity through possible regulation of hypothalamic neuropeptide secretion
Source and license
Adapted from rs16964476 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.