Rs11052552

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is asnp
is mentioned by
dbSNPrs11052552
hapmaprs11052552
hgdprs11052552
ensemblrs11052552
gopubmedrs11052552
scholarrs11052552
googlers11052552
pharmgkbrs11052552
hgvbaseg2prs11052552
medrefsnprs11052552
23andMers11052552
SNP Nexus

Chromosome12
Orientationplus
Position9747224
GenotypeEffect
rs11052552(G;G)1.4x risk
rs11052552(G;T)1.5x risk
rs11052552(T;T)normal


Genotypes Magnitude Summary
Rs11052552(G;G) 1.4x risk
Rs11052552(G;T) 1.5x risk
Rs11052552(T;T) 00 normal
rs11052552 has been reported in a large study to be associated with type-1 diabetes.

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.49 (CI 1.28-1.73), and for homozygotes, 1.43 (CI 1.21-1.69). [PMID 17554300]

? (G;G) (G;T) (T;T)
GWAS
SNP rs11052552
PubMedID [PMID 17554300]
Condition Type 1 diabetes
Gene NR
Risk Allele G
pValue 7.00E-007
OR 1.49
95% CI 1.28-1.73


PharmGKBPA162356637
Name
AnnotationGWAS Results: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (Initial Sample Size: 1,963 cases, 2,938 controls; Replication Sample Size: (see Todd 2007); Risk Allele: rs11052552-G). This variant is associated with type 1 diabetes.
Gene-
Featue
EvidencePubMed ID:17554300; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesDiabetes Mellitus, Diabetes Mellitus, Type 1
Curation LevelNon-Curated