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rs398123112(GGTGGCCCACGCCTACCGCCTCT;GGTGGCCCACGCCTACCGCCTCT)

From SNPedia
common in clinvar
Is agenotype
ofrs398123112
GeneABCD1, BCAP31
ChromosomeX
Position153,725,764
mentionedby
Magnitude0
ReputeGood
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