C1848805[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 7666	NM_000453.3(SLC5A5):c.799C>G (p.Gln267Glu)	SLC5A5 (Q267E)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely pathogenic
Select item 891419	NM_000453.3(SLC5A5):c.1421G>A (p.Arg474Lys)	SLC5A5 (R474K)	Single nucleotide variant (missense variant)	Familial thyroid dyshormonogenesis 1	GUncertain significance