Rs358806

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is asnp
is mentioned by
dbSNPrs358806
hapmaprs358806
hgdprs358806
ensemblrs358806
gopubmedrs358806
scholarrs358806
googlers358806
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hgvbaseg2prs358806
medrefsnprs358806
23andMers358806
SNP Nexus

Chromosome3
Orientationplus
Position55288439
GenotypeEffect
rs358806(A;A)normal risk of type-2 diabetes
rs358806(A;C)0.9x risk of type-2 diabetes
rs358806(C;C)1.8x risk of type-2 diabetes


Genotypes Magnitude Summary
Rs358806(A;A) normal risk of type-2 diabetes
Rs358806(A;C) 0.9x risk of type-2 diabetes
Rs358806(C;C) 1.8x risk of type-2 diabetes
rs358806 has been reported in a large study to be associated with type-2 diabetes. The risk allele is (C); the odds ratio associated with heterozygotes is 0.86 (CI 0.75-0.97), and for homozygotes, 1.78 (CI 1.34-2.36). [PMID 17554300]
? (A;A) (A;C) (C;C)
GWAS
SNP rs358806
PubMedID [PMID 17554300]
Condition Type 2 diabetes
Gene NR
Risk Allele
pValue 3.00E-006
OR 1.16
95% CI 1.03-1.33


PharmGKBPA162356507
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)). 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