rs11220082
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11220082(C;C) |
Make rs11220082(C;T) |
Make rs11220082(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 125454069 |
Gene | FEZ1 |
is a | snp |
is | mentioned by |
dbSNP | rs11220082 |
dbSNP (classic) | rs11220082 |
ClinGen | rs11220082 |
ebi | rs11220082 |
HLI | rs11220082 |
Exac | rs11220082 |
Gnomad | rs11220082 |
Varsome | rs11220082 |
LitVar | rs11220082 |
Map | rs11220082 |
PheGenI | rs11220082 |
Biobank | rs11220082 |
1000 genomes | rs11220082 |
hgdp | rs11220082 |
ensembl | rs11220082 |
geneview | rs11220082 |
scholar | rs11220082 |
rs11220082 | |
pharmgkb | rs11220082 |
gwascentral | rs11220082 |
openSNP | rs11220082 |
23andMe | rs11220082 |
SNPshot | rs11220082 |
SNPdbe | rs11220082 |
MSV3d | rs11220082 |
GWAS Ctlg | rs11220082 |
GMAF | 0.4706 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22688191![]() |
Trait | |
Title | Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. |
Risk Allele | |
P-val | 7E-7 |
Odds Ratio | 1.1000 None |