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rs16856187

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs16856187(A;C)
Make rs16856187(C;C)
ReferenceGRCh37 37.1/131
Chromosome2
Position168913876
is asnp
is mentioned by
dbSNPrs16856187
dbSNP (classic)rs16856187
ClinGenrs16856187
ebirs16856187
HLIrs16856187
Exacrs16856187
Gnomadrs16856187
Varsomers16856187
LitVarrs16856187
Maprs16856187
PheGenIrs16856187
Biobankrs16856187
1000 genomesrs16856187
hgdprs16856187
ensemblrs16856187
geneviewrs16856187
scholarrs16856187
googlers16856187
pharmgkbrs16856187
gwascentralrs16856187
openSNPrs16856187
23andMers16856187
SNPshotrs16856187
SNPdbers16856187
MSV3drs16856187
GWAS Ctlgrs16856187
GMAF0.135
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 19082990] type 2 diabetes and fasting plasma glucose concentration.


[PMID 20628598OA-icon.png] Common polymorphisms in MTNR1B, G6PC2 and GCK are associated with increased fasting plasma glucose and impaired beta-cell function in Chinese subjects.


[PMID 20668700OA-icon.png] Effects of GCK, GCKR, G6PC2 and MTNR1B variants on glucose metabolism and insulin secretion.