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rs17797882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17797882(C;T)
Make rs17797882(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position79373021
is asnp
is mentioned by
dbSNPrs17797882
ebirs17797882
HLIrs17797882
Exacrs17797882
Varsomers17797882
Maprs17797882
PheGenIrs17797882
hapmaprs17797882
1000 genomesrs17797882
hgdprs17797882
ensemblrs17797882
gopubmedrs17797882
geneviewrs17797882
scholarrs17797882
googlers17797882
pharmgkbrs17797882
gwascentralrs17797882
openSNPrs17797882
23andMers17797882
23andMe allrs17797882
SNP Nexus

SNPshotrs17797882
SNPdbers17797882
MSV3drs17797882
GWAS Ctlgrs17797882
GMAF0.09275
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22158537OA-icon.png]
Trait
Title Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.
Risk Allele T
P-val 9E-7
Odds Ratio 1.0800 None


[PMID 24086726OA-icon.png] Replication Study for the Association of 9 East Asian GWAS-Derived Loci with Susceptibility to Type 2 Diabetes in a Japanese Population