C4721531[trait identifier] AND "Johns Hopkins Genomics, Johns Hopkins - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 515337	NM_139276.3(STAT3):c.2288C>T (p.Ser763Leu)	STAT3 (S763L +9 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 2443043	NM_139276.3(STAT3):c.1004G>A (p.Arg335Gln)	STAT3 (R303Q +2 more)	Single nucleotide variant (missense variant)	Hyper-IgE recurrent infection syndrome 1, autosomal dominant +1 more	GUncertain significance