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rs104894639(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs104894639
GeneSGSH
Chromosome17
Position80,210,622
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 3 Carrier of a Sanfilippo syndrome type A mutation
(G;G) 0 common in clinvar