rs10892759
A SNP in the SORL1 gene on chromosome 11. Its most notable genotype is A;A: reduced risk for Alzheimers?
- Gene
- SORL1
- Location
- Chr 11121,593,379 (GRCh38)
- Highest magnitude
- 1.0Minor
- Tested on
- 23andMe
- Minor allele frequency
- 47%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (A;G), (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.
- AverageA;A 36% A;G 45% G;G 20%
- European ancestry (Utah)A;A 13% A;G 42% G;G 46%
- Han Chinese (Beijing)A;A 42% A;G 42% G;G 16%
- Japanese (Tokyo)A;A 41% A;G 44% G;G 15%
- Yoruba (Nigeria)A;A 43% A;G 43% G;G 14%
- African ancestry (Southwest US)A;A 37% A;G 47% G;G 16%
- Chinese (Denver)A;A 40% A;G 49% G;G 11%
- Gujarati IndianA;A 44% A;G 45% G;G 12%
- Luhya (Kenya)A;A 49% A;G 43% G;G 8%
- Mexican ancestry (Los Angeles)A;A 31% A;G 48% G;G 21%
- Maasai (Kenya)A;A 40% A;G 48% G;G 12%
- TuscanA;A 12% A;G 40% G;G 48%
Related
Other SORL1 SNPs
- rs1784931C;Creduced 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
- rs2298814G;Gcommon in complete genomicsTypical
Notes
From SNPedia
Notes
A;A
A single paper in 2007 found a link to reduced (0.83x) risk for Alzheimers.
Source and license
Adapted from rs10892759 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.