rs11252926
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11252926(C;C) |
Make rs11252926(C;T) |
Make rs11252926(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 520439 |
Gene | DIP2C |
is a | snp |
is | mentioned by |
dbSNP | rs11252926 |
dbSNP (classic) | rs11252926 |
ClinGen | rs11252926 |
ebi | rs11252926 |
HLI | rs11252926 |
Exac | rs11252926 |
Gnomad | rs11252926 |
Varsome | rs11252926 |
LitVar | rs11252926 |
Map | rs11252926 |
PheGenI | rs11252926 |
Biobank | rs11252926 |
1000 genomes | rs11252926 |
hgdp | rs11252926 |
ensembl | rs11252926 |
geneview | rs11252926 |
scholar | rs11252926 |
rs11252926 | |
pharmgkb | rs11252926 |
gwascentral | rs11252926 |
openSNP | rs11252926 |
23andMe | rs11252926 |
SNPshot | rs11252926 |
SNPdbe | rs11252926 |
MSV3d | rs11252926 |
GWAS Ctlg | rs11252926 |
GMAF | 0.202 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22005930![]() |
Trait | |
Title | Genome-wide association study of Alzheimer's disease with psychotic symptoms. |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | 1.3900 None |