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rs11066453

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs11066453(A;G)
Make rs11066453(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position112927816
is asnp
is mentioned by
dbSNPrs11066453
ebirs11066453
HLIrs11066453
Exacrs11066453
Varsomers11066453
Maprs11066453
PheGenIrs11066453
hapmaprs11066453
1000 genomesrs11066453
hgdprs11066453
ensemblrs11066453
gopubmedrs11066453
geneviewrs11066453
scholarrs11066453
googlers11066453
pharmgkbrs11066453
gwascentralrs11066453
openSNPrs11066453
23andMers11066453
23andMe allrs11066453
SNP Nexus

SNPshotrs11066453
SNPdbers11066453
MSV3drs11066453
GWAS Ctlgrs11066453
GMAF0.04178
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21909109]
Trait
Title Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits.
Risk Allele G
P-val 6E-44
Odds Ratio 0.0097 [0.0083-0.0111] IU/L increase
GWAS snp
PMID [PMID 23575436]
Trait Glycemic traits
Title New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population.
Risk Allele G
P-val 5E-9
Odds Ratio .24 [0.16-0.32] mmol-1 decrease