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rs104894549(C;C)

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common in clinvar

Is a	genotype
of	rs104894549
Gene	ASPA, SPATA22
Chromosome	17
Position	3,494,369
mentioned	by

0

Good

Geno	Mag	Summary
(A;A)	8	Canavan disease (predicted)
(A;C)	3	Carrier of a Canavan disease mutation
(C;C)	0	common in clinvar

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Is a genotype