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rs587776741(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs587776741
GeneTAZ
ChromosomeX
Position154,420,211
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;G) 3 carrier of a Barth syndrome allele
(G;G) 0 common in clinvar