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.