List of variants in gene STAT3 reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.1757T>C (p.Met586Thr)	rs1459473021	0.00001
NM_139276.3(STAT3):c.38G>A (p.Arg13Gln)	rs780720013	0.00001
NM_139276.3(STAT3):c.-23-1G>T
NM_139276.3(STAT3):c.1238T>A (p.Leu413Gln)
NM_139276.3(STAT3):c.1303G>A (p.Glu435Lys)	rs2144730363
NM_139276.3(STAT3):c.1339C>G (p.His447Asp)
NM_139276.3(STAT3):c.1366-15_1366-5del	rs1064796770
NM_139276.3(STAT3):c.2248G>C (p.Gly750Arg)	rs2144617568
NM_139276.3(STAT3):c.605A>G (p.Gln202Arg)	rs2144878191
NM_139276.3(STAT3):c.617T>G (p.Met206Arg)
NM_139276.3(STAT3):c.82A>G (p.Met28Val)	rs2145013673
NM_139276.3(STAT3):c.832C>T (p.Arg278Cys)	rs1555566945
NM_139276.3(STAT3):c.836A>C (p.Gln279Pro)
NM_139276.3(STAT3):c.952A>G (p.Lys318Glu)
NM_139276.3(STAT3):c.961T>G (p.Phe321Val)
NM_139276.3(STAT3):c.983G>T (p.Cys328Phe)

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