rs10770141
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10770141(A;A) |
| Make rs10770141(A;G) |
| Make rs10770141(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 2172610 |
| Gene | MIR4686, TH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10770141 |
| dbSNP (classic) | rs10770141 |
| ClinGen | rs10770141 |
| ebi | rs10770141 |
| HLI | rs10770141 |
| Exac | rs10770141 |
| Gnomad | rs10770141 |
| Varsome | rs10770141 |
| LitVar | rs10770141 |
| Map | rs10770141 |
| PheGenI | rs10770141 |
| Biobank | rs10770141 |
| 1000 genomes | rs10770141 |
| hgdp | rs10770141 |
| ensembl | rs10770141 |
| geneview | rs10770141 |
| scholar | rs10770141 |
| rs10770141 | |
| pharmgkb | rs10770141 |
| gwascentral | rs10770141 |
| openSNP | rs10770141 |
| 23andMe | rs10770141 |
| SNPshot | rs10770141 |
| SNPdbe | rs10770141 |
| MSV3d | rs10770141 |
| GWAS Ctlg | rs10770141 |
| GMAF | 0.3604 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 19958792] Association study between a functional polymorphism of tyrosine hydroxylase gene promoter and personality traits in healthy subjects
[PMID 20571875
] Human Tyrosine Hydroxylase Natural Allelic Variation: Influence on Autonomic Function and Hypertension
[PMID 17717598] Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk.
[PMID 18180394] Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans.
[PMID 23246742] Association of monoamine-synthesizing genes with the depression tendency and personality in chronic fatigue syndrome patients.
