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rs4753426

From SNPedia

Orientationplus
Stabilizedplus
Make rs4753426(C;C)
Make rs4753426(C;T)
Make rs4753426(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position92968430
GeneMTNR1B
is asnp
is mentioned by
dbSNPrs4753426
ebirs4753426
HLIrs4753426
Exacrs4753426
Varsomers4753426
Maprs4753426
PheGenIrs4753426
hapmaprs4753426
1000 genomesrs4753426
hgdprs4753426
ensemblrs4753426
gopubmedrs4753426
geneviewrs4753426
scholarrs4753426
googlers4753426
pharmgkbrs4753426
gwascentralrs4753426
openSNPrs4753426
23andMers4753426
23andMe allrs4753426
SNP Nexus

SNPshotrs4753426
SNPdbers4753426
MSV3drs4753426
GWAS Ctlgrs4753426
GMAF0.4431
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19088850OA-icon.png] Polymorphisms within the novel type 2 diabetes risk locus MTNR1B determine beta-cell function.


[PMID 21526376] Association of Polymorphism in the Promoter of the Melatonin Receptor 1A Gene with Schizophrenia and with Insomnia Symptoms in Schizophrenia Patients


[PMID 22698518] Melatonin pathway genes are associated with progressive subtypes and disability status in multiple sclerosis among Finnish patients


[PMID 17632395] Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.


[PMID 20050988] Association of disease-predisposition polymorphisms of the melatonin receptors and sunshine duration in the global human populations.


[PMID 21353709] Single nucleotide polymorphisms and mRNA expression for melatonin MT(2) receptor in depression.


[PMID 21711391] Association and evolutionary studies of the melatonin receptor 1B gene (MTNR1B) in the self-contained population of Sorbs from Germany.


[PMID 22759724] Polymorphisms in the melatonin receptor 1B gene and the risk of delirium


[PMID 23611530] Genetics of melatonin receptor type 2 is associated with left ventricular function in hypertensive patients treated according to guidelines.


[PMID 24969335] [Association between single nucleotide polymorphism of rs4753426 of melatonin receptor 1B gene and gestational diabetes mellitus]


[PMID 25898821] The polymorphisms of melatonin receptor 1B gene (MTNR1B) (rs4753426 and rs10830963) and susceptibility to adolescent idiopathic scoliosis: a meta-analysis