rs10277664
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10277664(C;C) |
| Make rs10277664(C;T) |
| Make rs10277664(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 139806781 |
| Gene | TBXAS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10277664 |
| dbSNP (classic) | rs10277664 |
| ClinGen | rs10277664 |
| ebi | rs10277664 |
| HLI | rs10277664 |
| Exac | rs10277664 |
| Gnomad | rs10277664 |
| Varsome | rs10277664 |
| LitVar | rs10277664 |
| Map | rs10277664 |
| PheGenI | rs10277664 |
| Biobank | rs10277664 |
| 1000 genomes | rs10277664 |
| hgdp | rs10277664 |
| ensembl | rs10277664 |
| geneview | rs10277664 |
| scholar | rs10277664 |
| rs10277664 | |
| pharmgkb | rs10277664 |
| gwascentral | rs10277664 |
| openSNP | rs10277664 |
| 23andMe | rs10277664 |
| SNPshot | rs10277664 |
| SNPdbe | rs10277664 |
| MSV3d | rs10277664 |
| GWAS Ctlg | rs10277664 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24086445 ]
|
| Trait | Gray matter volume (schizophrenia interaction) |
| Title | Genome-wide association analysis with gray matter volume as a quantitative phenotype in first-episode treatment-naïve patients with schizophrenia. |
| Risk Allele | |
| P-val | 1E-7 |
| Odds Ratio | .04 [NR] unit decrease |
