rs13189798
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13189798(A;A) |
| Make rs13189798(A;C) |
| Make rs13189798(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 76191426 |
| Gene | SV2C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13189798 |
| dbSNP (classic) | rs13189798 |
| ClinGen | rs13189798 |
| ebi | rs13189798 |
| HLI | rs13189798 |
| Exac | rs13189798 |
| Gnomad | rs13189798 |
| Varsome | rs13189798 |
| LitVar | rs13189798 |
| Map | rs13189798 |
| PheGenI | rs13189798 |
| Biobank | rs13189798 |
| 1000 genomes | rs13189798 |
| hgdp | rs13189798 |
| ensembl | rs13189798 |
| geneview | rs13189798 |
| scholar | rs13189798 |
| rs13189798 | |
| pharmgkb | rs13189798 |
| gwascentral | rs13189798 |
| openSNP | rs13189798 |
| 23andMe | rs13189798 |
| SNPshot | rs13189798 |
| SNPdbe | rs13189798 |
| MSV3d | rs13189798 |
| GWAS Ctlg | rs13189798 |
| Max Magnitude | 0 |
[PMID 25985399
] Associations of common variants in the BST2 region with HIV-1 acquisition in African American and European American people who inject drugs
