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