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rs4760790

From SNPedia

Orientationplus
Stabilizedplus
Make rs4760790(A;A)
Make rs4760790(A;G)
Make rs4760790(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position71241014
is asnp
is mentioned by
dbSNPrs4760790
ebirs4760790
HLIrs4760790
Exacrs4760790
Varsomers4760790
Maprs4760790
PheGenIrs4760790
hapmaprs4760790
1000 genomesrs4760790
hgdprs4760790
ensemblrs4760790
gopubmedrs4760790
geneviewrs4760790
scholarrs4760790
googlers4760790
pharmgkbrs4760790
gwascentralrs4760790
openSNPrs4760790
23andMers4760790
23andMe allrs4760790
SNP Nexus

SNPshotrs4760790
SNPdbers4760790
MSV3drs4760790
GWAS Ctlgrs4760790
GMAF0.2296
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20581827OA-icon.png]
Trait Type 2 diabetes
Title Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Risk Allele A
P-val 0.000004
Odds Ratio 1.11 [1.06-1.16]