Rs10896449

From SNPedia

Jump to: navigation, search
is asnp
is mentioned by
dbSNPrs10896449
hapmaprs10896449
hgdprs10896449
ensemblrs10896449
gopubmedrs10896449
scholarrs10896449
googlers10896449
pharmgkbrs10896449
hgvbaseg2prs10896449
medrefsnprs10896449
23andMers10896449
SNP Nexus

Chromosome11
Orientationplus
Position68751242
GenotypeEffect
rs10896449(A;A)*?
rs10896449(A;G)*?
rs10896449(G;G)*?


nature identifies rs10486567 rs10993994 rs10896449 in prostate cancer
Neighborrs7931342
Distance170
? (A;A) (A;G) (G;G)
GWAS
SNP rs10896449
PubMedID [PMID 18264096]
Condition Prostate cancer (aggressive)
Gene Intergenic
Risk Allele G
pValue 2.00E-009
OR 1.1
95% CI 0.98-1.23


[PMID 19505914] Two independent prostate cancer risk-associated Loci at 11q13

Related to PROSTATE CANCER, HEREDITARY, 14; HPC14 according to omim 611958. See also


[PMID 19902474] Replication of prostate cancer risk loci on 8q24, 11q13, 17q12, 19q33, and Xp11 in African Americans

PharmGKBPA162356742
Name
AnnotationGWAS Results: Multiple loci identified in a genome-wide association study of prostate cancer (Initial Sample Size: 1,172 cases, 1,157 controls; Replication Sample Size: 3,941 cases, 3,964 controls; Risk Allele: rs10896449-G).
Gene-
Featue
EvidencePubMed ID:18264096; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesProstatic Neoplasms
Curation LevelNon-Curated
Retrieved from "http://www.snpedia.com/index.php/Rs10896449"