rs111485003
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs111485003(A;A) |
| Make rs111485003(A;G) |
| Make rs111485003(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 154531696 |
| Gene | G6PD |
| is a | snp |
| is | mentioned by |
| dbSNP | rs111485003 |
| dbSNP (classic) | rs111485003 |
| ClinGen | rs111485003 |
| ebi | rs111485003 |
| HLI | rs111485003 |
| Exac | rs111485003 |
| Gnomad | rs111485003 |
| Varsome | rs111485003 |
| LitVar | rs111485003 |
| Map | rs111485003 |
| PheGenI | rs111485003 |
| Biobank | rs111485003 |
| 1000 genomes | rs111485003 |
| hgdp | rs111485003 |
| ensembl | rs111485003 |
| geneview | rs111485003 |
| scholar | rs111485003 |
| rs111485003 | |
| pharmgkb | rs111485003 |
| gwascentral | rs111485003 |
| openSNP | rs111485003 |
| 23andMe | rs111485003 |
| SNPshot | rs111485003 |
| SNPdbe | rs111485003 |
| MSV3d | rs111485003 |
| GWAS Ctlg | rs111485003 |
| Max Magnitude | 0 |
[PMID 23389243] 3'-UTR variations and G6PD deficiency
