Rs5945619

From SNPedia

Jump to: navigation, search
is asnp
is mentioned by
dbSNPrs5945619
hapmaprs5945619
hgdprs5945619
ensemblrs5945619
gopubmedrs5945619
scholarrs5945619
googlers5945619
pharmgkbrs5945619
hgvbaseg2prs5945619
medrefsnprs5945619
23andMers5945619
SNP Nexus

ChromosomeX
Orientationplus
Position51258411
GenotypeEffect
rs5945619(C;C)*?
rs5945619(C;T)*?
rs5945619(T;T)*?


cancer-genetics these snps influence genetic risk for prostate cancer

? (C;C) (C;T) (T;T)


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

[PMID 19366831] Analysis of Recently Identified Prostate Cancer Susceptibility Loci in a Population-based Study: Associations with Family History and Clinical Features

GWAS snp
PMID [PMID 18264097]
Trait Prostate cancer
Title Multiple newly identified loci associated with prostate cancer susceptibility
Risk Allele C
P-val 2.0000000000000001E-9
Odds Ratio 1.19 [1.07-1.31]


[PMID 19549809] Fine-Mapping and Family-Based Association Analyses of Prostate Cancer Risk Variants at Xp11

Related to PROSTATE CANCER, HEREDITARY, X-LINKED 2; HPCX2 according to omim 300704. See also