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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC5A5
(Q267E)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely pathogenic
SLC5A5
(R474K)
Single nucleotide variant
(missense variant)
Thyroid dyshormonogenesis 1
GUncertain significance