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rs193922098(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs193922098
GeneABCD1, BCAP31
ChromosomeX
Position153,726,104
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of X-linked adrenoleukodystrophy mutation; probably unaffected
(T;T) 7.7 X-linked adrenoleukodystrophy; symptoms and age of onset highly variable