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rs4065

From SNPedia

Orientationplus
Stabilizedplus
Make rs4065(C;C)
Make rs4065(C;T)
Make rs4065(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position73916706
GeneC10orf55, PLAU
is asnp
is mentioned by
dbSNPrs4065
ebirs4065
HLIrs4065
Exacrs4065
Varsomers4065
Maprs4065
PheGenIrs4065
hapmaprs4065
1000 genomesrs4065
hgdprs4065
ensemblrs4065
gopubmedrs4065
geneviewrs4065
scholarrs4065
googlers4065
pharmgkbrs4065
gwascentralrs4065
openSNPrs4065
23andMers4065
23andMe allrs4065
SNP Nexus

SNPshotrs4065
SNPdbers4065
MSV3drs4065
GWAS Ctlgrs4065
GMAF0.4178
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20937265] Association of polymorphisms in the genes of the urokinase plasminogen activation system with susceptibility to and severity of non-small cell lung cancer


[PMID 21761413] Genetic polymorphism of the plasminogen activator inhibitor-1 is associated with an increased risk of endometrial cancer


[PMID 16385451OA-icon.png] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.


[PMID 16967469] Association of tagSNPs in the urokinase-plasminogen activator (PLAU) gene with Alzheimer's disease and associated quantitative traits.


[PMID 17363771] Association of urokinase-type plasminogen activator with asthma and atopy.


[PMID 17601350OA-icon.png] A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.


[PMID 17994220] Association between urokinase haplotypes and outcome from infection-associated acute lung injury.


[PMID 18076107OA-icon.png] Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis.


[PMID 18988861OA-icon.png] Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes.


[PMID 19001172OA-icon.png] Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study: implication of additional loci.


[PMID 20518747] Association of putative functional variants in the PLAU gene and the PLAUR gene with myocardial infarction.