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rs1799836

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
Make rs1799836(A;A)
Make rs1799836(A;G)
Make rs1799836(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position43768752
GeneMAOB
is asnp
is mentioned by
dbSNPrs1799836
ebirs1799836
HLIrs1799836
Exacrs1799836
Varsomers1799836
Maprs1799836
PheGenIrs1799836
hapmaprs1799836
1000 genomesrs1799836
hgdprs1799836
ensemblrs1799836
gopubmedrs1799836
geneviewrs1799836
scholarrs1799836
googlers1799836
pharmgkbrs1799836
gwascentralrs1799836
openSNPrs1799836
23andMers1799836
23andMe allrs1799836
SNP Nexus

SNPshotrs1799836
SNPdbers1799836
MSV3drs1799836
GWAS Ctlgrs1799836
GMAF0.4311
Max Magnitude0
? (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 19657584OA-icon.png] Negative emotionality: monoamine oxidase B gene variants modulate personality traits in healthy humans


[PMID 21978760OA-icon.png] Association study of monoamine oxidase A/B genes and schizophrenia in Han Chinese


[PMID 16174289OA-icon.png] MAOA haplotypes associated with thrombocyte-MAO activity.


[PMID 16848906OA-icon.png] 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 18180394OA-icon.png] Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans.


[PMID 19018232OA-icon.png] Comparison of the genotyping results using DNA obtained from blood and saliva.


[PMID 19344875OA-icon.png] Association test for X-linked QTL in family-based designs.


[PMID 19772600OA-icon.png] 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]