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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TPO
(F289S)
Single nucleotide variant
(missense variant +1 more)
Congenital hypothyroidism
GPathogenic
TPO
Duplication
(splice donor variant +1 more)
Congenital hypothyroidism
GLikely pathogenic