rs9261129
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs9261129(C;C) |
| Make rs9261129(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 30011802 |
| Gene | HCG8, ZNRD1ASP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9261129 |
| dbSNP (classic) | rs9261129 |
| ClinGen | rs9261129 |
| ebi | rs9261129 |
| HLI | rs9261129 |
| Exac | rs9261129 |
| Gnomad | rs9261129 |
| Varsome | rs9261129 |
| LitVar | rs9261129 |
| Map | rs9261129 |
| PheGenI | rs9261129 |
| Biobank | rs9261129 |
| 1000 genomes | rs9261129 |
| hgdp | rs9261129 |
| ensembl | rs9261129 |
| geneview | rs9261129 |
| scholar | rs9261129 |
| rs9261129 | |
| pharmgkb | rs9261129 |
| gwascentral | rs9261129 |
| openSNP | rs9261129 |
| 23andMe | rs9261129 |
| SNPshot | rs9261129 |
| SNPdbe | rs9261129 |
| MSV3d | rs9261129 |
| GWAS Ctlg | rs9261129 |
| GMAF | 0.1846 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18495769
] Transmission of human immunodeficiency virus type 1 from a patient who developed AIDS to an elite suppressor.
[PMID 18982067] HIV-1 disease-influencing effects associated with ZNRD1, HCP5 and HLA-C alleles are attributable mainly to either HLA-A10 or HLA-B*57 alleles.
[PMID 20041166] Common genetic variation and the control of HIV-1 in humans.
