rs10793294
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10793294(A;A) |
| Make rs10793294(A;C) |
| Make rs10793294(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 78285357 |
| Gene | GAB2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10793294 |
| dbSNP (classic) | rs10793294 |
| ClinGen | rs10793294 |
| ebi | rs10793294 |
| HLI | rs10793294 |
| Exac | rs10793294 |
| Gnomad | rs10793294 |
| Varsome | rs10793294 |
| LitVar | rs10793294 |
| Map | rs10793294 |
| PheGenI | rs10793294 |
| Biobank | rs10793294 |
| 1000 genomes | rs10793294 |
| hgdp | rs10793294 |
| ensembl | rs10793294 |
| geneview | rs10793294 |
| scholar | rs10793294 |
| rs10793294 | |
| pharmgkb | rs10793294 |
| gwascentral | rs10793294 |
| openSNP | rs10793294 |
| 23andMe | rs10793294 |
| SNPshot | rs10793294 |
| SNPdbe | rs10793294 |
| MSV3d | rs10793294 |
| GWAS Ctlg | rs10793294 |
| GMAF | 0.4876 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 21108942] Common variant in GRB2 is associated with late-onset Alzheimer's disease in Han Chinese
[PMID 17553421
] GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.
[PMID 23071633] Mining pure, strict epistatic interactions from high-dimensional datasets: ameliorating the curse of dimensionality.
