rs2312147
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2312147(C;C) |
| Make rs2312147(C;T) |
| Make rs2312147(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 57995793 |
| Gene | VRK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2312147 |
| dbSNP (classic) | rs2312147 |
| ClinGen | rs2312147 |
| ebi | rs2312147 |
| HLI | rs2312147 |
| Exac | rs2312147 |
| Gnomad | rs2312147 |
| Varsome | rs2312147 |
| LitVar | rs2312147 |
| Map | rs2312147 |
| PheGenI | rs2312147 |
| Biobank | rs2312147 |
| 1000 genomes | rs2312147 |
| hgdp | rs2312147 |
| ensembl | rs2312147 |
| geneview | rs2312147 |
| scholar | rs2312147 |
| rs2312147 | |
| pharmgkb | rs2312147 |
| gwascentral | rs2312147 |
| openSNP | rs2312147 |
| 23andMe | rs2312147 |
| SNPshot | rs2312147 |
| SNPdbe | rs2312147 |
| MSV3d | rs2312147 |
| GWAS Ctlg | rs2312147 |
| GMAF | 0.2764 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19571808 ]
|
| Trait | Schizophrenia |
| Title | Common variants conferring risk of schizophrenia |
| Risk Allele | C |
| P-val | 3E-7 |
| Odds Ratio | 1.09 [NR] |
[PMID 21791550] Common variants at VRK2 and TCF4 conferring risk of schizophrenia.
[PMID 23102693] Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility.
[PMID 27382989] Further evidence of VRK2 rs2312147 associated with schizophrenia.
