rs121908978(A;G)
From SNPedia
| Carrier of a glycogen storage disease type Ib mutation |
| Is a | genotype |
| of | rs121908978 |
| Gene | SLC37A4 |
| Chromosome | 11 |
| Position | 119,029,287 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | Carrier of a glycogen storage disease type Ib mutation |
| (G;G) | 0 | common in clinvar |
Unaffected in absence of a second SLC37A4 gene mutation
