rs1799836
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs1799836(A;A) |
| Make rs1799836(A;G) |
| Make rs1799836(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 43768752 |
| Gene | MAOB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1799836 |
| dbSNP (classic) | rs1799836 |
| ClinGen | rs1799836 |
| ebi | rs1799836 |
| HLI | rs1799836 |
| Exac | rs1799836 |
| Gnomad | rs1799836 |
| Varsome | rs1799836 |
| LitVar | rs1799836 |
| Map | rs1799836 |
| PheGenI | rs1799836 |
| Biobank | rs1799836 |
| 1000 genomes | rs1799836 |
| hgdp | rs1799836 |
| ensembl | rs1799836 |
| geneview | rs1799836 |
| scholar | rs1799836 |
| rs1799836 | |
| pharmgkb | rs1799836 |
| gwascentral | rs1799836 |
| openSNP | rs1799836 |
| 23andMe | rs1799836 |
| SNPshot | rs1799836 |
| SNPdbe | rs1799836 |
| MSV3d | rs1799836 |
| GWAS Ctlg | rs1799836 |
| GMAF | 0.4311 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18205889] Parkinson's disease The risk alleles for each SNP identified from conditional logistic regression, rs1721100 C, rs1721082 T and rs1799836 A, are consistent with previous reports.
Significant interaction between this MAOB SNP and a FGF20 SNP, rs1721100 was also noticed.
[PMID 19657584
] Negative emotionality: monoamine oxidase B gene variants modulate personality traits in healthy humans
[PMID 21978760] Association study of monoamine oxidase A/B genes and schizophrenia in Han Chinese
[PMID 16174289] MAOA haplotypes associated with thrombocyte-MAO activity.
[PMID 16848906] Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.
[PMID 17427196] Monoamine oxidase A gene polymorphism predicts adolescent outcome of attention-deficit/hyperactivity disorder.
[PMID 17918234] The monoamine oxidase B gene exhibits significant association to ADHD.
[PMID 18180394] Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans.
[PMID 19018232] Comparison of the genotyping results using DNA obtained from blood and saliva.
[PMID 19344875] Association test for X-linked QTL in family-based designs.
[PMID 19772600] A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.
[PMID 23111930] MAOA and MAOB polymorphisms and anger-related traits in suicidal participants and controls
[PMID 25805645] Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson's disease
[PMID 25636089] [Polymorphisms of catechol-O-methyltransferase and monoamine oxidase B genes among Chinese patients with Parkinson's disease]
[PMID 29578580] MAO-B and COMT Genetic Variations Associated With Levodopa Treatment Response in Patients With Parkinson's Disease.
