rs979416826
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 | rs979416826 |
| dbSNP (classic) | rs979416826 |
| ClinGen | rs979416826 |
| ebi | rs979416826 |
| HLI | rs979416826 |
| Exac | rs979416826 |
| Gnomad | rs979416826 |
| Varsome | rs979416826 |
| LitVar | rs979416826 |
| Map | rs979416826 |
| PheGenI | rs979416826 |
| Biobank | rs979416826 |
| 1000 genomes | rs979416826 |
| hgdp | rs979416826 |
| ensembl | rs979416826 |
| geneview | rs979416826 |
| scholar | rs979416826 |
| rs979416826 | |
| pharmgkb | rs979416826 |
| gwascentral | rs979416826 |
| openSNP | rs979416826 |
| 23andMe | rs979416826 |
| SNPshot | rs979416826 |
| SNPdbe | rs979416826 |
| MSV3d | rs979416826 |
| GWAS Ctlg | rs979416826 |
| Max Magnitude | 5 |
aka c.406C>T, c.496C>T, (p.Arg136Cys or R136C)
