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rs398123105(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs398123105
GeneABCD1
ChromosomeX
Position153,740,618
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 4.4 Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible
(C;T) 4.4 Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible
(G;G) 7.7 X-linked adrenoleukodystrophy; symptoms and age of onset highly variable
(T;T) 7.7 X-linked adrenoleukodystrophy; symptoms and age of onset highly variable