rs433598
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs433598(C;C) |
| Make rs433598(C;T) |
| Make rs433598(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 20668884 |
| Gene | ACSM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs433598 |
| dbSNP (classic) | rs433598 |
| ClinGen | rs433598 |
| ebi | rs433598 |
| HLI | rs433598 |
| Exac | rs433598 |
| Gnomad | rs433598 |
| Varsome | rs433598 |
| LitVar | rs433598 |
| Map | rs433598 |
| PheGenI | rs433598 |
| Biobank | rs433598 |
| 1000 genomes | rs433598 |
| hgdp | rs433598 |
| ensembl | rs433598 |
| geneview | rs433598 |
| scholar | rs433598 |
| rs433598 | |
| pharmgkb | rs433598 |
| gwascentral | rs433598 |
| openSNP | rs433598 |
| 23andMe | rs433598 |
| SNPshot | rs433598 |
| SNPdbe | rs433598 |
| MSV3d | rs433598 |
| GWAS Ctlg | rs433598 |
| GMAF | 0.4096 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20185149 ]
|
| Trait | Schizophrenia |
| Title | Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. |
| Risk Allele | T |
| P-val | 0.000003 |
| Odds Ratio | 1.13 [NR] |
[PMID 25656805] Genetic association of ACSM1 variation with schizophrenia and major depressive disorder in the Han Chinese population
