rs203332
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs203332(A;A) |
Make rs203332(A;G) |
Make rs203332(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 119772533 |
Gene | CIT |
is a | snp |
is | mentioned by |
dbSNP | rs203332 |
dbSNP (classic) | rs203332 |
ClinGen | rs203332 |
ebi | rs203332 |
HLI | rs203332 |
Exac | rs203332 |
Gnomad | rs203332 |
Varsome | rs203332 |
LitVar | rs203332 |
Map | rs203332 |
PheGenI | rs203332 |
Biobank | rs203332 |
1000 genomes | rs203332 |
hgdp | rs203332 |
ensembl | rs203332 |
geneview | rs203332 |
scholar | rs203332 |
rs203332 | |
pharmgkb | rs203332 |
gwascentral | rs203332 |
openSNP | rs203332 |
23andMe | rs203332 |
SNPshot | rs203332 |
SNPdbe | rs203332 |
MSV3d | rs203332 |
GWAS Ctlg | rs203332 |
GMAF | 0.483 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20084519] Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging