rs1386498
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1386498(A;A) |
| Make rs1386498(A;G) |
| Make rs1386498(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 72004363 |
| Gene | TPH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1386498 |
| dbSNP (classic) | rs1386498 |
| ClinGen | rs1386498 |
| ebi | rs1386498 |
| HLI | rs1386498 |
| Exac | rs1386498 |
| Gnomad | rs1386498 |
| Varsome | rs1386498 |
| LitVar | rs1386498 |
| Map | rs1386498 |
| PheGenI | rs1386498 |
| Biobank | rs1386498 |
| 1000 genomes | rs1386498 |
| hgdp | rs1386498 |
| ensembl | rs1386498 |
| geneview | rs1386498 |
| scholar | rs1386498 |
| rs1386498 | |
| pharmgkb | rs1386498 |
| gwascentral | rs1386498 |
| openSNP | rs1386498 |
| 23andMe | rs1386498 |
| SNPshot | rs1386498 |
| SNPdbe | rs1386498 |
| MSV3d | rs1386498 |
| GWAS Ctlg | rs1386498 |
| GMAF | 0.4986 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 21396719] Influence of TPH2 variants on diagnosis and response to treatment in patients with major depression, bipolar disorder and schizophrenia
