rs10263087
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10263087(C;C) |
| Make rs10263087(C;G) |
| Make rs10263087(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 155178759 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10263087 |
| dbSNP (classic) | rs10263087 |
| ClinGen | rs10263087 |
| ebi | rs10263087 |
| HLI | rs10263087 |
| Exac | rs10263087 |
| Gnomad | rs10263087 |
| Varsome | rs10263087 |
| LitVar | rs10263087 |
| Map | rs10263087 |
| PheGenI | rs10263087 |
| Biobank | rs10263087 |
| 1000 genomes | rs10263087 |
| hgdp | rs10263087 |
| ensembl | rs10263087 |
| geneview | rs10263087 |
| scholar | rs10263087 |
| rs10263087 | |
| pharmgkb | rs10263087 |
| gwascentral | rs10263087 |
| openSNP | rs10263087 |
| 23andMe | rs10263087 |
| SNPshot | rs10263087 |
| SNPdbe | rs10263087 |
| MSV3d | rs10263087 |
| GWAS Ctlg | rs10263087 |
| GMAF | 0.1777 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22648509] |
| Trait | |
| Title | PKNOX2 is Associated with Formal Thought Disorder in Schizophrenia: a Meta-Analysis of Two Genome-wide Association Studies. |
| Risk Allele | C |
| P-val | 0.000007 |
| Odds Ratio | 1.5470 None |
