rs4751185
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs4751185(C;T) |
| Make rs4751185(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 130258151 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4751185 |
| dbSNP (classic) | rs4751185 |
| ClinGen | rs4751185 |
| ebi | rs4751185 |
| HLI | rs4751185 |
| Exac | rs4751185 |
| Gnomad | rs4751185 |
| Varsome | rs4751185 |
| LitVar | rs4751185 |
| Map | rs4751185 |
| PheGenI | rs4751185 |
| Biobank | rs4751185 |
| 1000 genomes | rs4751185 |
| hgdp | rs4751185 |
| ensembl | rs4751185 |
| geneview | rs4751185 |
| scholar | rs4751185 |
| rs4751185 | |
| pharmgkb | rs4751185 |
| gwascentral | rs4751185 |
| openSNP | rs4751185 |
| 23andMe | rs4751185 |
| SNPshot | rs4751185 |
| SNPdbe | rs4751185 |
| MSV3d | rs4751185 |
| GWAS Ctlg | rs4751185 |
| GMAF | 0.1065 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21160409 ]
|
| Trait | |
| Title | Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population |
| Risk Allele | |
| P-val | 0.000007 |
| Odds Ratio | None None |
