rs9368699
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs9368699(C;C) |
| Make rs9368699(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31834764 |
| Gene | C6orf48, SNORD48 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9368699 |
| dbSNP (classic) | rs9368699 |
| ClinGen | rs9368699 |
| ebi | rs9368699 |
| HLI | rs9368699 |
| Exac | rs9368699 |
| Gnomad | rs9368699 |
| Varsome | rs9368699 |
| LitVar | rs9368699 |
| Map | rs9368699 |
| PheGenI | rs9368699 |
| Biobank | rs9368699 |
| 1000 genomes | rs9368699 |
| hgdp | rs9368699 |
| ensembl | rs9368699 |
| geneview | rs9368699 |
| scholar | rs9368699 |
| rs9368699 | |
| pharmgkb | rs9368699 |
| gwascentral | rs9368699 |
| openSNP | rs9368699 |
| 23andMe | rs9368699 |
| SNPshot | rs9368699 |
| SNPdbe | rs9368699 |
| MSV3d | rs9368699 |
| GWAS Ctlg | rs9368699 |
| GMAF | 0.06887 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20041166 ]
|
| Trait | HIV-1 control |
| Title | Common Genetic Variation and the Control of HIV-1 in Human |
| Risk Allele | |
| P-val | 5E-8 |
| Odds Ratio | NR NR |
[PMID 22238471] Single-nucleotide polymorphism-defined class I and class III major histocompatibility complex genetic subregions contribute to natural long-term nonprogression in HIV infection.
