rs9333289
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9333289(C;C) |
| Make rs9333289(C;T) |
| Make rs9333289(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 186633380 |
| Gene | ITGAV |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9333289 |
| dbSNP (classic) | rs9333289 |
| ClinGen | rs9333289 |
| ebi | rs9333289 |
| HLI | rs9333289 |
| Exac | rs9333289 |
| Gnomad | rs9333289 |
| Varsome | rs9333289 |
| LitVar | rs9333289 |
| Map | rs9333289 |
| PheGenI | rs9333289 |
| Biobank | rs9333289 |
| 1000 genomes | rs9333289 |
| hgdp | rs9333289 |
| ensembl | rs9333289 |
| geneview | rs9333289 |
| scholar | rs9333289 |
| rs9333289 | |
| pharmgkb | rs9333289 |
| gwascentral | rs9333289 |
| openSNP | rs9333289 |
| 23andMe | rs9333289 |
| SNPshot | rs9333289 |
| SNPdbe | rs9333289 |
| MSV3d | rs9333289 |
| GWAS Ctlg | rs9333289 |
| GMAF | 0.1827 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
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[PMID 14681825
] Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).
