rs11179027
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11179027(C;C) |
| Make rs11179027(C;G) |
| Make rs11179027(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 71983532 |
| Gene | TPH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11179027 |
| dbSNP (classic) | rs11179027 |
| ClinGen | rs11179027 |
| ebi | rs11179027 |
| HLI | rs11179027 |
| Exac | rs11179027 |
| Gnomad | rs11179027 |
| Varsome | rs11179027 |
| LitVar | rs11179027 |
| Map | rs11179027 |
| PheGenI | rs11179027 |
| Biobank | rs11179027 |
| 1000 genomes | rs11179027 |
| hgdp | rs11179027 |
| ensembl | rs11179027 |
| geneview | rs11179027 |
| scholar | rs11179027 |
| rs11179027 | |
| pharmgkb | rs11179027 |
| gwascentral | rs11179027 |
| openSNP | rs11179027 |
| 23andMe | rs11179027 |
| SNPshot | rs11179027 |
| SNPdbe | rs11179027 |
| MSV3d | rs11179027 |
| GWAS Ctlg | rs11179027 |
| GMAF | 0.3315 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21396719] Influence of TPH2 variants on diagnosis and response to treatment in patients with major depression, bipolar disorder and schizophrenia
[PMID 23337130] Common genetic background in anorexia nervosa and obsessive compulsive disorder: preliminary results from an association study.
[PMID 23461725] Association between TPH2 gene polymorphisms and attention deficit hyperactivity disorder in Korean children.
