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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HAAO
(W186*)
Single nucleotide variant
(nonsense)
Congenital NAD deficiency disorder
+1 more
GPathogenic
HAAO
(D162*)
Duplication
(nonsense)
Congenital NAD deficiency disorder
+1 more
GPathogenic