rs10494326
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10494326(C;T) |
| Make rs10494326(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 159679910 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10494326 |
| dbSNP (classic) | rs10494326 |
| ClinGen | rs10494326 |
| ebi | rs10494326 |
| HLI | rs10494326 |
| Exac | rs10494326 |
| Gnomad | rs10494326 |
| Varsome | rs10494326 |
| LitVar | rs10494326 |
| Map | rs10494326 |
| PheGenI | rs10494326 |
| Biobank | rs10494326 |
| 1000 genomes | rs10494326 |
| hgdp | rs10494326 |
| ensembl | rs10494326 |
| geneview | rs10494326 |
| scholar | rs10494326 |
| rs10494326 | |
| pharmgkb | rs10494326 |
| gwascentral | rs10494326 |
| openSNP | rs10494326 |
| 23andMe | rs10494326 |
| SNPshot | rs10494326 |
| SNPdbe | rs10494326 |
| MSV3d | rs10494326 |
| GWAS Ctlg | rs10494326 |
| Merged from | Rs16827466 |
| GMAF | 0.04178 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 17564960
] A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population.
