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rs104894636(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs104894636
GeneSGSH
Chromosome17
Position80,217,061
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a Sanfilippo syndrome type A mutation