rs1557229683
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| (C;T) | 3 | Carrier of G6PD deficiency mutation; variable expressivity |
| (T;T) | 5 | G6PD deficiency |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1557229683 |
| dbSNP (classic) | rs1557229683 |
| ClinGen | rs1557229683 |
| ebi | rs1557229683 |
| HLI | rs1557229683 |
| Exac | rs1557229683 |
| Gnomad | rs1557229683 |
| Varsome | rs1557229683 |
| LitVar | rs1557229683 |
| Map | rs1557229683 |
| PheGenI | rs1557229683 |
| Biobank | rs1557229683 |
| 1000 genomes | rs1557229683 |
| hgdp | rs1557229683 |
| ensembl | rs1557229683 |
| geneview | rs1557229683 |
| scholar | rs1557229683 |
| rs1557229683 | |
| pharmgkb | rs1557229683 |
| gwascentral | rs1557229683 |
| openSNP | rs1557229683 |
| 23andMe | rs1557229683 |
| SNPshot | rs1557229683 |
| SNPdbe | rs1557229683 |
| MSV3d | rs1557229683 |
| GWAS Ctlg | rs1557229683 |
| Max Magnitude | 5 |
aka c.1187C>T, c.1277C>T, (p.Pro396Leu or P396L)
