rs3800569
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3800569(A;A) |
| Make rs3800569(A;G) |
| Make rs3800569(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 138726680 |
| Gene | ATP6V0A4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3800569 |
| dbSNP (classic) | rs3800569 |
| ClinGen | rs3800569 |
| ebi | rs3800569 |
| HLI | rs3800569 |
| Exac | rs3800569 |
| Gnomad | rs3800569 |
| Varsome | rs3800569 |
| LitVar | rs3800569 |
| Map | rs3800569 |
| PheGenI | rs3800569 |
| Biobank | rs3800569 |
| 1000 genomes | rs3800569 |
| hgdp | rs3800569 |
| ensembl | rs3800569 |
| geneview | rs3800569 |
| scholar | rs3800569 |
| rs3800569 | |
| pharmgkb | rs3800569 |
| gwascentral | rs3800569 |
| openSNP | rs3800569 |
| 23andMe | rs3800569 |
| SNPshot | rs3800569 |
| SNPdbe | rs3800569 |
| MSV3d | rs3800569 |
| GWAS Ctlg | rs3800569 |
| GMAF | 0.2094 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21326311 ]
|
| Trait | |
| Title | Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients |
| Risk Allele | C |
| P-val | 0.000006 |
| Odds Ratio | 1.2000 [0.69-1.71] unit increase |
