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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GCH1, LOC130055692
(V6L)
Single nucleotide variant
(missense variant)
Dystonia 5
+2 more
GUncertain significance
GCH1, LOC130055692
Single nucleotide variant
(5 prime UTR variant)
Dystonia 5
+2 more
GUncertain significance