rs387906709(C;C)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs387906709 |
| Gene | UBQLN2 |
| Chromosome | X |
| Position | 56,565,363 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 7.9 | Amyotrophic lateral sclerosis, type 15 |
| (A;C) | 7.9 | Amyotrophic lateral sclerosis, type 15 |
| (C;C) | 0 | common in clinvar |
| (C;T) | 7.9 | Heterogenous neurodegeneration disorder |
| (T;T) | 7.9 | Heterogeneous neurodegeneration disorder |
