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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TG
(G77S)
Single nucleotide variant
(missense variant)
TG-related disorder
+4 more
GConflicting classifications of pathogenicity
TG
(C1728*)
Single nucleotide variant
(nonsense)
Iodotyrosyl coupling defect
+1 more
GPathogenic