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rs104894433(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs104894433
GeneGCH1
Chromosome14
Position54,902,402
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 4.4 dystonia due on GCH1 loss-of-function mutation