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rs344781

From SNPedia

Orientationplus
Stabilizedplus
Make rs344781(C;C)
Make rs344781(C;T)
Make rs344781(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position43670636
GenePLAUR
is asnp
is mentioned by
dbSNPrs344781
ebirs344781
HLIrs344781
Exacrs344781
Varsomers344781
Maprs344781
PheGenIrs344781
hapmaprs344781
1000 genomesrs344781
hgdprs344781
ensemblrs344781
gopubmedrs344781
geneviewrs344781
scholarrs344781
googlers344781
pharmgkbrs344781
gwascentralrs344781
openSNPrs344781
23andMers344781
23andMe allrs344781
SNP Nexus

SNPshotrs344781
SNPdbers344781
MSV3drs344781
GWAS Ctlgrs344781
GMAF0.2511
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19360663OA-icon.png] Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder


[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 20967855] A genetic variation located in the promoter of the uPAR (CD87) gene is associated with the vascular complications of systemic sclerosis


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


[PMID 19552680OA-icon.png] Common hemostasis and inflammation gene variants and venous thrombosis in older adults from the Cardiovascular Health Study.


[PMID 19878584OA-icon.png] PLAUR polymorphisms and lung function in UK smokers.


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