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rs104894442(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs104894442
GeneGCH1
Chromosome14
Position54,844,023
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 4 dystonia due to autosomal recessive GCH1 mutation
(G;G) 0 common in clinvar