Rs7931342

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is asnp
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dbSNPrs7931342
hapmaprs7931342
hgdprs7931342
ensemblrs7931342
gopubmedrs7931342
scholarrs7931342
googlers7931342
pharmgkbrs7931342
hgvbaseg2prs7931342
medrefsnprs7931342
23andMers7931342
SNP Nexus

Chromosome11
Orientationplus
Position68751072
GenotypeEffect
rs7931342(G;G)*?
rs7931342(G;T)*?
rs7931342(T;T)*?


cancer-genetics these snps influence genetic risk for prostate cancer

[PMID 18974127] rs7931342 showed some evidence of association with breast cancer (per minor allele OR, 0.95; 95% CI, 0.91-0.99; P(trend) = 0.028)

Neighborrs10896449
Distance170
? (G;G) (G;T) (T;T)
GWAS
SNP rs7931342
PubMedID [PMID 18264097]
Condition Prostate cancer
Gene Intergenic
Risk Allele G
pValue 2.00E-012
OR 1.19
95% CI 1.11-1.27


[PMID 19336566] Replication of the 10q11 and Xp11 Prostate Cancer Risk Variants: Results from a Utah Pedigree-Based Study.

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


PharmGKBPA162356748
Name
AnnotationGWAS Results: Multiple newly identified loci associated with prostate cancer susceptibility (Initial Sample Size: 1,854 cases, 1,894 controls; Replication Sample Size: 3,268 cases, 3,366 controls; Risk Allele: rs7931342-G).
Gene-
Featue
EvidencePubMed ID:18264097; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesProstatic Neoplasms
Curation LevelNon-Curated