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rs104894441(T;T)

From SNPedia
common in clinvar
Is agenotype
ofrs104894441
GeneGCH1
Chromosome14
Position54,865,376
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;T) 4.4 dystonia due on GCH1 loss-of-function mutation
(T;T) 0 common in clinvar