rs11042950
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs11042950(A;A) |
| Make rs11042950(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 2168488 |
| Gene | TH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11042950 |
| dbSNP (classic) | rs11042950 |
| ClinGen | rs11042950 |
| ebi | rs11042950 |
| HLI | rs11042950 |
| Exac | rs11042950 |
| Gnomad | rs11042950 |
| Varsome | rs11042950 |
| LitVar | rs11042950 |
| Map | rs11042950 |
| PheGenI | rs11042950 |
| Biobank | rs11042950 |
| 1000 genomes | rs11042950 |
| hgdp | rs11042950 |
| ensembl | rs11042950 |
| geneview | rs11042950 |
| scholar | rs11042950 |
| rs11042950 | |
| pharmgkb | rs11042950 |
| gwascentral | rs11042950 |
| openSNP | rs11042950 |
| 23andMe | rs11042950 |
| SNPshot | rs11042950 |
| SNPdbe | rs11042950 |
| MSV3d | rs11042950 |
| GWAS Ctlg | rs11042950 |
| GMAF | 0.002755 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24275212] The role of tyrosine hydroxylase gene variants in suicide attempt in schizophrenia
| ClinVar | |
|---|---|
| Risk | rs11042950(A;A) |
| Alt | rs11042950(A;A) |
| Reference | Rs11042950(G;G) |
| Significance | Non-pathogenic |
| Disease | Dystonia |
| Variation | info |
| Gene | TH |
| CLNDBN | Dystonia |
| Reversed | 1 |
| HGVS | NC_000011.9:g.2189718C>T |
| CLNSRC | |
| CLNACC | RCV000229985.1, |
