rs9610449
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9610449(C;C) |
| Make rs9610449(C;T) |
| Make rs9610449(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 36215187 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9610449 |
| dbSNP (classic) | rs9610449 |
| ClinGen | rs9610449 |
| ebi | rs9610449 |
| HLI | rs9610449 |
| Exac | rs9610449 |
| Gnomad | rs9610449 |
| Varsome | rs9610449 |
| LitVar | rs9610449 |
| Map | rs9610449 |
| PheGenI | rs9610449 |
| Biobank | rs9610449 |
| 1000 genomes | rs9610449 |
| hgdp | rs9610449 |
| ensembl | rs9610449 |
| geneview | rs9610449 |
| scholar | rs9610449 |
| rs9610449 | |
| pharmgkb | rs9610449 |
| gwascentral | rs9610449 |
| openSNP | rs9610449 |
| 23andMe | rs9610449 |
| SNPshot | rs9610449 |
| SNPdbe | rs9610449 |
| MSV3d | rs9610449 |
| GWAS Ctlg | rs9610449 |
| GMAF | 0.2475 |
| Max Magnitude | 0 |
[PMID 18632255
] rs9610449 schizophrenia (377 families, 1161 genotyped members and 647 genotyped affected in total) rs9610449 and rs6000200 associated with risk for schizophrenia in African-Americans. In the combined (AA and EA) sample, two SNPs, rs2003813 and rs2157249
