"Fulgent Genetics, Fulgent Genetics"[submitter] AND "THOC2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 788159	NM_001081550.2(THOC2):c.4338A>G (p.Pro1446=)	THOC2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 716737	NM_001081550.2(THOC2):c.1261G>A (p.Ala421Thr)	THOC2 (A421T)	Single nucleotide variant (missense variant)	X-linked intellectual disability-short stature-overweight syndrome +1 more	GBenign/Likely benign