RS886039379 GCH1

Health Risk Chr 14:54844138
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What This Variant Does
"CLNSIG=5
Associated Conditions
Dystonia 5
GTP cyclohydrolase I deficiency
Inborn genetic diseases
Dystonia 5
GTP cyclohydrolase I deficiency
Inborn genetic diseases
Other Variants in GCH1
rs104894433 rs104894437 rs2140127822 rs104894438 rs2140074226 rs104894439 rs104894440 rs2140073990 rs2140074192 rs104894434
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