rs682748
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs682748(C;C) |
| Make rs682748(C;T) |
| Make rs682748(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 17148802 |
| Gene | LOC285696 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs682748 |
| dbSNP (classic) | rs682748 |
| ClinGen | rs682748 |
| ebi | rs682748 |
| HLI | rs682748 |
| Exac | rs682748 |
| Gnomad | rs682748 |
| Varsome | rs682748 |
| LitVar | rs682748 |
| Map | rs682748 |
| PheGenI | rs682748 |
| Biobank | rs682748 |
| 1000 genomes | rs682748 |
| hgdp | rs682748 |
| ensembl | rs682748 |
| geneview | rs682748 |
| scholar | rs682748 |
| rs682748 | |
| pharmgkb | rs682748 |
| gwascentral | rs682748 |
| openSNP | rs682748 |
| 23andMe | rs682748 |
| SNPshot | rs682748 |
| SNPdbe | rs682748 |
| MSV3d | rs682748 |
| GWAS Ctlg | rs682748 |
| GMAF | 0.4858 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19668339 ]
|
| Trait | Hippocampal atrophy |
| Title | Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease |
| Risk Allele | |
| P-val | 0.000008 |
| Odds Ratio | NR NR |
