rs4450776
A SNP in the PLCXD2 gene on chromosome 3. Its most notable genotype is C;C: common on affy axiom data
- Gene
- PLCXD2
- Location
- Chr 3111,704,282 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 6%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). 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.
- AverageC;C 87%
- European ancestry (Utah)C;C 91%
- Han Chinese (Beijing)C;C 84%
- Japanese (Tokyo)C;C 86%
- Yoruba (Nigeria)C;C 86%
Notes
From SNPedia
Notes
non sig. gwas, hit (p = 5 x 10^-6) for PC1 (principal component 1) among the cognitive tests performed
Source and license
Adapted from rs4450776 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.