rs10489202
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10489202(G;G) |
| Make rs10489202(G;T) |
| Make rs10489202(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 167933841 |
| Gene | MPC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10489202 |
| dbSNP (classic) | rs10489202 |
| ClinGen | rs10489202 |
| ebi | rs10489202 |
| HLI | rs10489202 |
| Exac | rs10489202 |
| Gnomad | rs10489202 |
| Varsome | rs10489202 |
| LitVar | rs10489202 |
| Map | rs10489202 |
| PheGenI | rs10489202 |
| Biobank | rs10489202 |
| 1000 genomes | rs10489202 |
| hgdp | rs10489202 |
| ensembl | rs10489202 |
| geneview | rs10489202 |
| scholar | rs10489202 |
| rs10489202 | |
| pharmgkb | rs10489202 |
| gwascentral | rs10489202 |
| openSNP | rs10489202 |
| 23andMe | rs10489202 |
| SNPshot | rs10489202 |
| SNPdbe | rs10489202 |
| MSV3d | rs10489202 |
| GWAS Ctlg | rs10489202 |
| GMAF | 0.1772 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22037555 ]
|
| Trait | |
| Title | Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. |
| Risk Allele | A |
| P-val | 1E-8 |
| Odds Ratio | 1.2300 None |
[PMID 23933155] Lack of association between MPC2 variants and schizophrenia in a replication study of Han Chinese
[PMID 30087317] Genetic association and meta-analysis of a schizophrenia GWAS variant rs10489202 in East Asian populations.
