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rs104894637(C;C)

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common in clinvar

Is a	genotype
of	rs104894637
Gene	SGSH
Chromosome	17
Position	80,217,084
mentioned	by

0

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	3	Carrier of a Sanfilippo syndrome type A mutation
(G;G)	8	Sanfilippo syndrome type A

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Is a genotype