rs786203009(T;T)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs786203009 |
| Gene | MAX, LOC100506321 |
| Chromosome | 14 |
| Position | 65,093,706 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (A;T) | 6.2 | Hereditary PGL/PCC Syndrome |
| (T;T) | 0 | common in clinvar |
