rs3203713
A SNP in the PLCE1 gene on chromosome 10. Its most notable genotype is A;A: common in clinvar
- Gene
- PLCE1
- Location
- Chr 1094,327,971 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA
- Minor allele frequency
- 10%
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 89%
- European ancestry (Utah)A;A 76%
- Han Chinese (Beijing)A;A 100%
- Japanese (Tokyo)A;A 100%
- Yoruba (Nigeria)A;A 78%
Related
Other PLCE1 SNPs
- rs2274223G;G1.9x increased risk for stomach & esophageal cancer (seen in Han Chinese)Worth knowing
- rs2274224G;Gcommon in clinvarTypical
- rs3765524C;Ccommon in clinvarTypical
- rs11187837T;Tcommon in complete genomicsTypical
- rs11187870G;Gcommon in complete genomicsTypical
- rs17417407G;Gcommon in clinvarTypical
Source and license
Adapted from rs3203713 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.