rs17646665
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common/normal |
| (A;G) | 3.9 | Moderately reduced risk for Alzheimer's (~0.6x) |
| (G;G) | 4.2 | Reduced risk for Alzheimer's (~0.33x?) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 1 |
| Position | 109369429 |
| Gene | SORT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17646665 |
| dbSNP (classic) | rs17646665 |
| ClinGen | rs17646665 |
| ebi | rs17646665 |
| HLI | rs17646665 |
| Exac | rs17646665 |
| Gnomad | rs17646665 |
| Varsome | rs17646665 |
| LitVar | rs17646665 |
| Map | rs17646665 |
| PheGenI | rs17646665 |
| Biobank | rs17646665 |
| 1000 genomes | rs17646665 |
| hgdp | rs17646665 |
| ensembl | rs17646665 |
| geneview | rs17646665 |
| scholar | rs17646665 |
| rs17646665 | |
| pharmgkb | rs17646665 |
| gwascentral | rs17646665 |
| openSNP | rs17646665 |
| 23andMe | rs17646665 |
| SNPshot | rs17646665 |
| SNPdbe | rs17646665 |
| MSV3d | rs17646665 |
| GWAS Ctlg | rs17646665 |
| Max Magnitude | 4.2 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 27392867
] A Genetic Variant of the Sortilin 1 Gene is Associated with Reduced Risk of Alzheimer's Disease. Minor Allele (G) associated with reduced risk (OR 0.6x, CI: 0.4-0.8) for Alzheimer's Disease; it is possible that the reported association could be restricted to a Swedish/Scandinavian population.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 1
- Has genotype
- Has population
- On chip 23andMe v3
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Affy GenomeWide 6
- On chip 23andMe v1
- On chip 23andMe v2
- On chip FTDNA
- On chip FTDNA2
- On chip 23andMe v4
- On chip Ancestry v2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
