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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129934069, SPR
Single nucleotide variant
(5 prime UTR variant)
not provided
+1 more
GBenign/Likely benign
LOC129934069, SPR
(G6R)
Single nucleotide variant
(missense variant)
Dopa-responsive dystonia due to sepiapterin reductase deficiency
+1 more
GUncertain significance
SPR
(R150G)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
SPR
(M218I)
Single nucleotide variant
(missense variant)
Dystonic disorder
+2 more
GUncertain significance
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