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rs193922097(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs193922097
GeneABCD1, BCAP31
ChromosomeX
Position153,725,687
mentionedby
Magnitude0
ReputeGood
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