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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TG
(R283Q)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
TG
(R2242H)
Single nucleotide variant
(missense variant)
Autoimmune thyroid disease, susceptibility to, 3
+2 more
GPathogenic