List of variants in gene STAT3 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.2082T>A (p.His694Gln)	rs139701269	0.00011
NM_139276.3(STAT3):c.1049+9T>G	rs374408588	0.00003
NM_139276.3(STAT3):c.1919A>T (p.Tyr640Phe)	rs769031989	0.00001
NM_139276.3(STAT3):c.1981G>T (p.Asp661Tyr)	rs747639500	0.00001
NM_139276.3(STAT3):c.368C>T (p.Ala123Val)	rs1475754644	0.00001
NM_139276.3(STAT3):c.372+10G>C	rs766222549	0.00001
NM_139276.3(STAT3):c.1229A>G (p.His410Arg)	rs2144772044
NM_139276.3(STAT3):c.1366-20A>G	rs1567710255
NM_139276.3(STAT3):c.1840A>C (p.Ser614Arg)	rs886039546
NM_139276.3(STAT3):c.1849G>A (p.Gly617Arg)	rs2144691698
NM_139276.3(STAT3):c.1852G>C (p.Gly618Arg)	rs2081548277
NM_139276.3(STAT3):c.1863C>G (p.Phe621Leu)	rs1555563854
NM_139276.3(STAT3):c.1919_1920delinsTT (p.Tyr640Phe)	rs2081522163
NM_139276.3(STAT3):c.1940A>T (p.Asn647Ile)	rs770986654
NM_139276.3(STAT3):c.1940_1941delinsTT (p.Asn647Ile)
NM_139276.3(STAT3):c.2144+46_2144+47del	rs1279773038
NM_139276.3(STAT3):c.2144+9C>G
STAT3:c.1601-72_1601-71del	rs149538586

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