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rs104894941(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs104894941
GeneTAZ, DNASE1L1
ChromosomeX
Position154,412,129
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 carrier of a Barth syndrome allele