rs6000200
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6000200(C;C) |
| Make rs6000200(C;G) |
| Make rs6000200(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 36216212 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6000200 |
| dbSNP (classic) | rs6000200 |
| ClinGen | rs6000200 |
| ebi | rs6000200 |
| HLI | rs6000200 |
| Exac | rs6000200 |
| Gnomad | rs6000200 |
| Varsome | rs6000200 |
| LitVar | rs6000200 |
| Map | rs6000200 |
| PheGenI | rs6000200 |
| Biobank | rs6000200 |
| 1000 genomes | rs6000200 |
| hgdp | rs6000200 |
| ensembl | rs6000200 |
| geneview | rs6000200 |
| scholar | rs6000200 |
| rs6000200 | |
| pharmgkb | rs6000200 |
| gwascentral | rs6000200 |
| openSNP | rs6000200 |
| 23andMe | rs6000200 |
| SNPshot | rs6000200 |
| SNPdbe | rs6000200 |
| MSV3d | rs6000200 |
| GWAS Ctlg | rs6000200 |
| GMAF | 0.2475 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[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
