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rs104894439(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs104894439
GeneGCH1
Chromosome14
Position54,902,661
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;G) 4 dystonia due on GCH1 loss-of-function mutation
(G;G) 0 common in clinvar