{{Rsnum
|rsid=2166706
|Chromosome=11
|position=92958366
|Orientation=plus
|GMAF=0.472
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 14.2 | 49.6 | 36.3
| HCB | 11.7 | 54.7 | 33.6
| JPT | 22.1 | 46.9 | 31.0
| YRI | 49.0 | 42.9 | 8.2
| ASW | 36.8 | 50.9 | 12.3
| CHB | 11.7 | 54.7 | 33.6
| CHD | 26.6 | 46.8 | 26.6
| GIH | 19.8 | 48.5 | 31.7
| LWK | 52.7 | 35.5 | 11.8
| MEX | 12.1 | 50.0 | 37.9
| MKK | 33.3 | 47.4 | 19.2
| TSI | 18.6 | 50.0 | 31.4
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19651812
|Title=Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type-2 diabetes amongst Indian Asians and European whites
|OA=1
}}

{{PMID Auto
|PMID=22768333
|Title=Association of Genetic Variants of Melatonin Receptor 1B with Gestational Plasma Glucose Level and Risk of Glucose Intolerance in Pregnant Chinese Women
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2166706
|overall_frequency_n=64
|overall_frequency_d=126
|overall_frequency=0.507936
|n_genomes=39
|n_genomes_annotated=0
|n_haplomes=55
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}