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rs104894435(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs104894435
GeneGCH1
Chromosome14
Position54,902,341
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 4 dystonia due to autosomal recessive GCH1 mutation
(A;G) 3 Carrier of a dopa-responsive dystonia mutation
(G;G) 0 common in clinvar