Rs12304921

From SNPedia

Jump to: navigation, search
is asnp
is mentioned by
dbSNPrs12304921
hapmaprs12304921
hgdprs12304921
ensemblrs12304921
gopubmedrs12304921
scholarrs12304921
googlers12304921
pharmgkbrs12304921
hgvbaseg2prs12304921
medrefsnprs12304921
23andMers12304921
SNP Nexus

Chromosome12
Orientationplus
Position49643808
GenotypeEffect
rs12304921(G;G)1.9x risk
rs12304921(A;G)2.5x risk
rs12304921(A;A)normal


Genotypes Magnitude Summary
Rs12304921(A;A) 00 normal
Rs12304921(A;G) 2.5x risk
Rs12304921(G;G) 1.9x risk

rs12304921 has been reported in a large study to be associated with type-2 diabetes.

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 2.50 (CI 1.53-4.09), and for homozygotes, 1.94 (CI 1.20-3.15). [PMID 17554300]

? (A;A) (A;G) (G;G)
GWAS
SNP rs12304921
PubMedID [PMID 17554300]
Condition Type 2 diabetes
Gene NR
Risk Allele G
pValue 7.00E-006
OR 2.5
95% CI 1.53-4.09


PharmGKBPA162356640
Name
AnnotationGWAS Results: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (Initial Sample Size: 1,924 cases, 2,938 controls; Replication Sample Size: (see Zeggini 2007); Risk Allele: rs12304921-G). This variant is associated with type 2 diabetes.
Gene-
Featue
EvidencePubMed ID:17554300; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesDiabetes Mellitus, Diabetes Mellitus, Type 2
Curation LevelNon-Curated