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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DPYD-AS1, DPYD
(P786H)
Single nucleotide variant
(missense variant)
Dihydropyrimidine dehydrogenase deficiency
GUncertain significance
DPYD
(P86L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic