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rs66626662(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs66626662
GeneOTC
ChromosomeX
Position38,401,372
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 8.2 Ornithine Transcarbamylase Deficiency
(A;G) 3 Carrier of an ornithine carbamoyltransferase mutation
(G;G) 0 common in clinvar