Rs3825932

From SNPedia

Jump to: navigation, search
is asnp
is mentioned by
dbSNPrs3825932
hapmaprs3825932
hgdprs3825932
ensemblrs3825932
gopubmedrs3825932
scholarrs3825932
googlers3825932
pharmgkbrs3825932
hgvbaseg2prs3825932
medrefsnprs3825932
23andMers3825932
SNP Nexus

Chromosome15
Orientationplus
Position77022500
GenotypeEffect
rs3825932(C;C)*?
rs3825932(C;T)*?
rs3825932(T;T)*?


GWAS snp
PMID [PMID 18978792]
Trait Type 1 diabetes
Title Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci
Risk Allele C
P-val 2.9999999999999998E-15
Odds Ratio 1.16 [1.10-1.22]
? (C;C) (C;T) (T;T)
GWAS snp
PMID [PMID 19430480]
Trait Type 1 diabetes
Title Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
Risk Allele
P-val 8E-8
Odds Ratio NR NR
Related to DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM according to omim 222100. See also


PharmGKBPA164740751
Name
AnnotationGWAS results: Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. (Initial Sample Size: 3,561 cases, 4,646 controls; Replication Sample Size: 6,225 cases, 6,946 controls, 3,064 trios); (Region: 15q25.1; Reported Gene(s): CTSH; Risk Allele: rs3825932-C); (p-value= 2.99999999999999E-15).This variant is associated with Type 1 diabetes.
GeneCTSH
Featue
EvidencePubMed ID:18978792; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesDiabetes Mellitus, Diabetes Mellitus, Type 1
Curation LevelNon-Curated