rs4919862
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4919862(C;C) |
| Make rs4919862(C;T) |
| Make rs4919862(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 19 |
| Position | 582253 |
| Gene | BSG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4919862 |
| dbSNP (classic) | rs4919862 |
| ClinGen | rs4919862 |
| ebi | rs4919862 |
| HLI | rs4919862 |
| Exac | rs4919862 |
| Gnomad | rs4919862 |
| Varsome | rs4919862 |
| LitVar | rs4919862 |
| Map | rs4919862 |
| PheGenI | rs4919862 |
| Biobank | rs4919862 |
| 1000 genomes | rs4919862 |
| hgdp | rs4919862 |
| ensembl | rs4919862 |
| geneview | rs4919862 |
| scholar | rs4919862 |
| rs4919862 | |
| pharmgkb | rs4919862 |
| gwascentral | rs4919862 |
| openSNP | rs4919862 |
| 23andMe | rs4919862 |
| SNPshot | rs4919862 |
| SNPdbe | rs4919862 |
| MSV3d | rs4919862 |
| GWAS Ctlg | rs4919862 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 28582638] Association of CD147 genetic polymorphisms with carotid atherosclerotic plaques in a Han Chinese population with cerebral infarction.
[PMID 32390081] The Single Nucleotide Polymorphisms of Chromosome 9p21 and CD147 Were Relevant with the Carotid Plaque Risk in Acute Cerebral Infarction Patients Among Chinese Han Population.
