rs10119
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs10119(C;C) |
| Make rs10119(C;T) |
| Make rs10119(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 19 |
| Position | 44903416 |
| Gene | TOMM40 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10119 |
| dbSNP (classic) | rs10119 |
| ClinGen | rs10119 |
| ebi | rs10119 |
| HLI | rs10119 |
| Exac | rs10119 |
| Gnomad | rs10119 |
| Varsome | rs10119 |
| LitVar | rs10119 |
| Map | rs10119 |
| PheGenI | rs10119 |
| Biobank | rs10119 |
| 1000 genomes | rs10119 |
| hgdp | rs10119 |
| ensembl | rs10119 |
| geneview | rs10119 |
| scholar | rs10119 |
| rs10119 | |
| pharmgkb | rs10119 |
| gwascentral | rs10119 |
| openSNP | rs10119 |
| 23andMe | rs10119 |
| SNPshot | rs10119 |
| SNPdbe | rs10119 |
| MSV3d | rs10119 |
| GWAS Ctlg | rs10119 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25644384
] Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)
[PMID 32725468] TOMM40 and APOE variants synergistically increase the risk of Alzheimer's disease in a Chinese population.
