RS104894435 GCH1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Dystonia 5
GTP cyclohydrolase I deficiency
Dystonia
dopa-responsive
with or without hyperphenylalaninemia
autosomal recessive
Dystonia 5
GTP cyclohydrolase I deficiency
Dystonia
dopa-responsive
with or without hyperphenylalaninemia
autosomal recessive
Other Variants in GCH1