rs10506645
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10506645(C;C) |
| Make rs10506645(C;T) |
| Make rs10506645(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 71991720 |
| Gene | TPH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10506645 |
| dbSNP (classic) | rs10506645 |
| ClinGen | rs10506645 |
| ebi | rs10506645 |
| HLI | rs10506645 |
| Exac | rs10506645 |
| Gnomad | rs10506645 |
| Varsome | rs10506645 |
| LitVar | rs10506645 |
| Map | rs10506645 |
| PheGenI | rs10506645 |
| Biobank | rs10506645 |
| 1000 genomes | rs10506645 |
| hgdp | rs10506645 |
| ensembl | rs10506645 |
| geneview | rs10506645 |
| scholar | rs10506645 |
| rs10506645 | |
| pharmgkb | rs10506645 |
| gwascentral | rs10506645 |
| openSNP | rs10506645 |
| 23andMe | rs10506645 |
| SNPshot | rs10506645 |
| SNPdbe | rs10506645 |
| MSV3d | rs10506645 |
| GWAS Ctlg | rs10506645 |
| GMAF | 0.2893 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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[PMID 19800079] Association of polymorphisms of the tryptophan hydroxylase 2 gene with risk for bipolar disorder or suicidal behavior
[PMID 22698518] Melatonin pathway genes are associated with progressive subtypes and disability status in multiple sclerosis among Finnish patients
[PMID 19184136
] Examination of association of genes in the serotonin system to autism.
[PMID 21085052] Association study of tryptophan hydroxylase 2 gene polymorphisms in bipolar disorder patients with panic disorder comorbidity.
[PMID 21412658] Associations between polymorphic variants of the tryptophan hydroxylase 2 gene and obsessive-compulsive disorder.
