rs11677416
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11677416(C;C) |
Make rs11677416(C;T) |
Make rs11677416(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 112771663 |
is a | snp |
is | mentioned by |
dbSNP | rs11677416 |
dbSNP (classic) | rs11677416 |
ClinGen | rs11677416 |
ebi | rs11677416 |
HLI | rs11677416 |
Exac | rs11677416 |
Gnomad | rs11677416 |
Varsome | rs11677416 |
LitVar | rs11677416 |
Map | rs11677416 |
PheGenI | rs11677416 |
Biobank | rs11677416 |
1000 genomes | rs11677416 |
hgdp | rs11677416 |
ensembl | rs11677416 |
geneview | rs11677416 |
scholar | rs11677416 |
rs11677416 | |
pharmgkb | rs11677416 |
gwascentral | rs11677416 |
openSNP | rs11677416 |
23andMe | rs11677416 |
SNPshot | rs11677416 |
SNPdbe | rs11677416 |
MSV3d | rs11677416 |
GWAS Ctlg | rs11677416 |
GMAF | 0.2029 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21107309] |
Trait | |
Title | Genome-Wide Pharmacogenomic Study of Neurocognition As an Indicator of Antipsychotic Treatment Response in Schizophrenia |
Risk Allele | |
P-val | 7E-7 |
Odds Ratio | None None |