List of variants in gene STAT3 reported as uncertain significance for autoimmune disease, multisystem, infantile-onset

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.2049C>T (p.Phe683=)	rs373256669	0.00017
NM_139276.3(STAT3):c.2228G>T (p.Gly743Val)	rs151033214	0.00011
NM_139276.3(STAT3):c.1233+19C>T	rs764434579	0.00010
NM_139276.3(STAT3):c.1887C>T (p.Ser629=)	rs769658142	0.00001
NM_139276.3(STAT3):c.373C>G (p.Gln125Glu)	rs574370336	0.00001
NM_139276.3(STAT3):c.1004G>A (p.Arg335Gln)
NM_139276.3(STAT3):c.1129G>A (p.Ala377Thr)	rs2081912356
NM_139276.3(STAT3):c.1333G>A (p.Val445Met)
NM_139276.3(STAT3):c.1339C>G (p.His447Asp)
NM_139276.3(STAT3):c.1749-4C>A
NM_139276.3(STAT3):c.1840A>C (p.Ser614Arg)	rs886039546
NM_139276.3(STAT3):c.1842C>G (p.Ser614Arg)
NM_139276.3(STAT3):c.2258-2A>G

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