rs80338788(G;G)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs80338788 |
| Gene | SCN4A, LOC105371858 |
| Chromosome | 17 |
| Position | 63,959,269 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | possibility of Hypokalemic periodic paralysis |
| (G;G) | 0 | common in clinvar |
