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rs104894942(A;C)

From SNPedia
carrier of a Barth syndrome allele
Is agenotype
ofrs104894942
GeneTAZ, DNASE1L1
ChromosomeX
Position154,413,248
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;C) 3 carrier of a Barth syndrome allele
(C;C) 0 common in clinvar

see discussion at rs104894942