rs440299
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs440299(A;A) |
| Make rs440299(A;G) |
| Make rs440299(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 119782478 |
| Gene | CIT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs440299 |
| dbSNP (classic) | rs440299 |
| ClinGen | rs440299 |
| ebi | rs440299 |
| HLI | rs440299 |
| Exac | rs440299 |
| Gnomad | rs440299 |
| Varsome | rs440299 |
| LitVar | rs440299 |
| Map | rs440299 |
| PheGenI | rs440299 |
| Biobank | rs440299 |
| 1000 genomes | rs440299 |
| hgdp | rs440299 |
| ensembl | rs440299 |
| geneview | rs440299 |
| scholar | rs440299 |
| rs440299 | |
| pharmgkb | rs440299 |
| gwascentral | rs440299 |
| openSNP | rs440299 |
| 23andMe | rs440299 |
| SNPshot | rs440299 |
| SNPdbe | rs440299 |
| MSV3d | rs440299 |
| GWAS Ctlg | rs440299 |
| GMAF | 0.4408 |
| 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
