rs1784919
A SNP in the SORL1 gene on chromosome 11. Its most notable genotype is C;C: common in complete genomics
- Gene
- SORL1
- Location
- Chr 11121,568,956 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 6%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs1784919 on the minus strand: (G;G). 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 84%
- European ancestry (Utah)C;C 97%
- Han Chinese (Beijing)C;C 93%
- Japanese (Tokyo)C;C 67%
- Yoruba (Nigeria)C;C 78%
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
- rs1792113A;AnormalTypical
- rs1792124G;Gcommon in complete genomicsTypical
- rs2298814G;Gcommon in complete genomicsTypical
Source and license
Adapted from rs1784919 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.