rs6808835
A SNP in the CCRL2 gene on chromosome 3. Its most notable genotype is G;G: common in complete genomics
- Gene
- CCRL2
- Location
- Chr 346,408,373 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 15%
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 2 HapMap populations.
- AverageG;G 52%
- European ancestry (Utah)G;G 77%
- Yoruba (Nigeria)G;G 27%
Source and license
Adapted from rs6808835 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.