rs6589885
A SNP in the SORL1 gene on chromosome 11. Its most notable genotype is G;G: common in complete genomics
- Gene
- SORL1
- Location
- Chr 11121,555,333 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 5%
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 11 HapMap populations.
- AverageG;G 88%
- European ancestry (Utah)G;G 96%
- Han Chinese (Beijing)G;G 88%
- Japanese (Tokyo)G;G 74%
- Yoruba (Nigeria)G;G 91%
- African ancestry (Southwest US)G;G 83%
- Chinese (Denver)G;G 85%
- Gujarati IndianG;G 95%
- Luhya (Kenya)G;G 80%
- Mexican ancestry (Los Angeles)G;G 93%
- Maasai (Kenya)G;G 87%
- TuscanG;G 97%
Related
Other SORL1 SNPs
- rs1784931C;Creduced risk for Alzheimers?Minor
- rs10892759A;Areduced risk for Alzheimers?Minor
- rs720099T;Tcommon in complete genomicsTypical
- rs726601C;CnormalTypical
- rs1699103T;TnormalTypical
- rs1784919C;Ccommon in complete genomicsTypical
- rs1792113A;AnormalTypical
- rs1792124G;Gcommon in complete genomicsTypical
Source and license
Adapted from rs6589885 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.