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rs104894635(G;G)

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common in clinvar

Is a	genotype
of	rs104894635
Gene	SGSH
Chromosome	17
Position	80,213,815
mentioned	by

0

Good

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

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Is a genotype