List of variants in gene STAT3 reported as not provided

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.1268G>A (p.Arg423Gln)	rs113994137	0.00001
NM_139276.3(STAT3):c.1140-2A>C	rs137854908
NM_139276.3(STAT3):c.1144C>T (p.Arg382Trp)	rs113994135
NM_139276.3(STAT3):c.1145G>A (p.Arg382Gln)	rs113994136
NM_139276.3(STAT3):c.1250G>T (p.Arg417Ile)	rs2144767285
NM_139276.3(STAT3):c.1384GTG[1] (p.Val463del)	rs113994138
NM_139276.3(STAT3):c.1601-10dup	rs3830585
NM_139276.3(STAT3):c.1909G>A (p.Val637Met)	rs113994139
NM_139276.3(STAT3):c.875C>G (p.Ser292Cys)	rs1598415625

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