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