rs373145711(C;T)
From SNPedia
| Bohring-Opitz syndrome |
| Is a | genotype |
| of | rs373145711 |
| Gene | ASXL1 |
| Chromosome | 20 |
| Position | 32,433,408 |
| mentioned | by |
| Magnitude | 8 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 8 | Bohring-Opitz syndrome |
see rs373145711
