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rs2166706

From SNPedia

Orientationplus
Stabilizedplus
Make rs2166706(C;C)
Make rs2166706(C;T)
Make rs2166706(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position92958366
is asnp
is mentioned by
dbSNPrs2166706
ebirs2166706
HLIrs2166706
Exacrs2166706
Varsomers2166706
Maprs2166706
PheGenIrs2166706
hapmaprs2166706
1000 genomesrs2166706
hgdprs2166706
ensemblrs2166706
gopubmedrs2166706
geneviewrs2166706
scholarrs2166706
googlers2166706
pharmgkbrs2166706
gwascentralrs2166706
openSNPrs2166706
23andMers2166706
23andMe allrs2166706
SNP Nexus

SNPshotrs2166706
SNPdbers2166706
MSV3drs2166706
GWAS Ctlgrs2166706
GMAF0.472
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19651812OA-icon.png] 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


[PMID 22768333OA-icon.png] Association of Genetic Variants of Melatonin Receptor 1B with Gestational Plasma Glucose Level and Risk of Glucose Intolerance in Pregnant Chinese Women


GET Evidence
rs2166706
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507936
summary