rs1318772
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1318772(A;A) |
| Make rs1318772(A;G) |
| Make rs1318772(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 113387870 |
| Gene | MCC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1318772 |
| dbSNP (classic) | rs1318772 |
| ClinGen | rs1318772 |
| ebi | rs1318772 |
| HLI | rs1318772 |
| Exac | rs1318772 |
| Gnomad | rs1318772 |
| Varsome | rs1318772 |
| LitVar | rs1318772 |
| Map | rs1318772 |
| PheGenI | rs1318772 |
| Biobank | rs1318772 |
| 1000 genomes | rs1318772 |
| hgdp | rs1318772 |
| ensembl | rs1318772 |
| geneview | rs1318772 |
| scholar | rs1318772 |
| rs1318772 | |
| pharmgkb | rs1318772 |
| gwascentral | rs1318772 |
| openSNP | rs1318772 |
| 23andMe | rs1318772 |
| SNPshot | rs1318772 |
| SNPdbe | rs1318772 |
| MSV3d | rs1318772 |
| GWAS Ctlg | rs1318772 |
| GMAF | 0.1423 |
| 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 | G |
| P-val | 0.000001 |
| Odds Ratio | 0.9100 [0.54-1.28] unit decrease |
