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rs104894434(C;C)

From SNPedia

dystonia due to autosomal recessive GCH1 mutation
Is agenotype
ofrs104894434
GeneGCH1
Chromosome14
Position54,844,108
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(C;C) 4 dystonia due to autosomal recessive GCH1 mutation
(T;T) 0 common in clinvar

The degree of dystonia may vary. See the SNPedia GCH1 page for discussion.