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rs398123103(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs398123103
GeneABCD1
ChromosomeX
Position153,740,189
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 7.7 Possible miscall by Ancestry; otherwise: X-linked adrenoleukodystrophy; symptoms and age of onset highly variable
(A;G) 4.4 Possible miscall by Ancestry; otherwise: Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible
(G;G) 0 common in clinvar