rs398123112(TCTGGTGGCCCACGCCTACCGCC;TCTGGTGGCCCACGCCTACCGCC)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs398123112 |
| Gene | ABCD1, BCAP31 |
| Chromosome | X |
| Position | 153,725,764 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 7.7 | X-linked adrenoleukodystrophy; symptoms and age of onset highly variable |
| (-;GGTGGCCCACGCCTACCGCCTCT) | 4.4 | Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible |
| (GGTGGCCCACGCCTACCGCCTCT;GGTGGCCCACGCCTACCGCCTCT) | 0 | common in clinvar |
| (TCTGGTGGCCCACGCCTACCGCC;TCTGGTGGCCCACGCCTACCGCC) | 0 | common in clinvar |
