rs4251805
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs4251805(A;A) |
| Make rs4251805(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 43670289 |
| Gene | PLAUR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4251805 |
| dbSNP (classic) | rs4251805 |
| ClinGen | rs4251805 |
| ebi | rs4251805 |
| HLI | rs4251805 |
| Exac | rs4251805 |
| Gnomad | rs4251805 |
| Varsome | rs4251805 |
| LitVar | rs4251805 |
| Map | rs4251805 |
| PheGenI | rs4251805 |
| Biobank | rs4251805 |
| 1000 genomes | rs4251805 |
| hgdp | rs4251805 |
| ensembl | rs4251805 |
| geneview | rs4251805 |
| scholar | rs4251805 |
| rs4251805 | |
| pharmgkb | rs4251805 |
| gwascentral | rs4251805 |
| openSNP | rs4251805 |
| 23andMe | rs4251805 |
| SNPshot | rs4251805 |
| SNPdbe | rs4251805 |
| MSV3d | rs4251805 |
| GWAS Ctlg | rs4251805 |
| GMAF | 0.03214 |
| Max Magnitude | 0 |
[PMID 20967855] A genetic variation located in the promoter of the uPAR (CD87) gene is associated with the vascular complications of systemic sclerosis
[PMID 19360663
] Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.
[PMID 19878584] PLAUR polymorphisms and lung function in UK smokers.
