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rs104894551(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs104894551
GeneASPA, SPATA22
Chromosome17
Position3,476,230
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 Carrier of a Canavan disease mutation
(G;G) 8 Canavan disease (predicted)