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rs104894942(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs104894942
GeneTAZ, DNASE1L1
ChromosomeX
Position154,413,248
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 3 carrier of a Barth syndrome allele
(C;C) 0 common in clinvar