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rs296766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs296766(C;T)
Make rs296766(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position49957170
GeneAQP2, LOC101927318
is asnp
is mentioned by
dbSNPrs296766
ebirs296766
HLIrs296766
Exacrs296766
Varsomers296766
Maprs296766
PheGenIrs296766
hapmaprs296766
1000 genomesrs296766
hgdprs296766
ensemblrs296766
gopubmedrs296766
geneviewrs296766
scholarrs296766
googlers296766
pharmgkbrs296766
gwascentralrs296766
openSNPrs296766
23andMers296766
23andMe allrs296766
SNP Nexus

SNPshotrs296766
SNPdbers296766
MSV3drs296766
GWAS Ctlgrs296766
GMAF0.1084
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 21934636] Genetic predisposition and nongenetic risk factors of thiazolidinedione-related edema in patients with type 2 diabetes