rs398123102(G;G)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs398123102 |
Gene | ABCD1 |
Chromosome | X |
Position | 153,740,156 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(A;A) | 7.7 | X-linked adrenoleukodystrophy; symptoms and age of onset highly variable |
(A;G) | 4.4 | Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible |
(G;G) | 0 | common in clinvar |