rs11187007
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11187007(A;A) |
| Make rs11187007(A;G) |
| Make rs11187007(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 92454823 |
| Gene | IDE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11187007 |
| dbSNP (classic) | rs11187007 |
| ClinGen | rs11187007 |
| ebi | rs11187007 |
| HLI | rs11187007 |
| Exac | rs11187007 |
| Gnomad | rs11187007 |
| Varsome | rs11187007 |
| LitVar | rs11187007 |
| Map | rs11187007 |
| PheGenI | rs11187007 |
| Biobank | rs11187007 |
| 1000 genomes | rs11187007 |
| hgdp | rs11187007 |
| ensembl | rs11187007 |
| geneview | rs11187007 |
| scholar | rs11187007 |
| rs11187007 | |
| pharmgkb | rs11187007 |
| gwascentral | rs11187007 |
| openSNP | rs11187007 |
| 23andMe | rs11187007 |
| SNPshot | rs11187007 |
| SNPdbe | rs11187007 |
| MSV3d | rs11187007 |
| GWAS Ctlg | rs11187007 |
| GMAF | 0.3696 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20927120] Variations in/nearby genes coding for JAZF1, TSPAN8/LGR5 and HHEX-IDE and risk of type 2 diabetes in Han Chinese [PMID 16675064] Weak independent association signals between IDE polymorphisms, Alzheimer's disease and cognitive measures.
