"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "STAT5A" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 731253	NM_001288718.2(STAT5A):c.465G>A (p.Thr155=)	STAT5A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 785569	NM_001288718.2(STAT5A):c.626T>C (p.Val209Ala)	STAT5A (V179A +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 735034	NM_001288718.2(STAT5A):c.1794G>C (p.Val598=)	STAT5A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 768884	NM_001288718.2(STAT5A):c.2063-4A>G	STAT5A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 789092	NM_001288718.2(STAT5A):c.2229C>T (p.Asp743=)	STAT5A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 785570	NM_001288718.2(STAT5A):c.2238C>T (p.Leu746=)	STAT5A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2425817	NC_000017.10:g.(?_40376777)_(40575115_?)dup	CAVIN1, STAT3 +2 more	Duplication	Growth hormone insensitivity with immune dysregulation 1, autosomal recessive +2 more	GUncertain significance

ClinVar