Have questions? Visit https://www.reddit.com/r/SNPedia

rs4251805

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs4251805(A;A)
Make rs4251805(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position43670289
GenePLAUR
is asnp
is mentioned by
dbSNPrs4251805
ebirs4251805
HLIrs4251805
Exacrs4251805
Varsomers4251805
Maprs4251805
PheGenIrs4251805
hapmaprs4251805
1000 genomesrs4251805
hgdprs4251805
ensemblrs4251805
gopubmedrs4251805
geneviewrs4251805
scholarrs4251805
googlers4251805
pharmgkbrs4251805
gwascentralrs4251805
openSNPrs4251805
23andMers4251805
23andMe allrs4251805
SNP Nexus

SNPshotrs4251805
SNPdbers4251805
MSV3drs4251805
GWAS Ctlgrs4251805
GMAF0.03214
Max Magnitude0

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


[PMID 19360663OA-icon.png] Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.


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