List of variants in gene STAT3 reported as pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.1919A>T (p.Tyr640Phe)	rs769031989	0.00001
NM_139276.3(STAT3):c.1139+1G>T	rs1598406623
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.1384GTG[1] (p.Val463del)	rs113994138
NM_139276.3(STAT3):c.1397A>G (p.Asn466Ser)	rs1057521091
NM_139276.3(STAT3):c.1840A>G (p.Ser614Gly)	rs886039546
NM_139276.3(STAT3):c.1909G>A (p.Val637Met)	rs113994139
NM_139276.3(STAT3):c.1940A>T (p.Asn647Ile)	rs770986654
NM_139276.3(STAT3):c.1979T>C (p.Met660Thr)	rs886039434
NM_139276.3(STAT3):c.2144C>T (p.Pro715Leu)	rs1064794957
NM_139276.3(STAT3):c.2147C>T (p.Thr716Met)	rs869312892
NM_139276.3(STAT3):c.454C>T (p.Arg152Trp)	rs869312890
NM_139276.3(STAT3):c.988C>T (p.Pro330Ser)
NM_139276.3(STAT3):c.994C>T (p.His332Tyr)	rs2144827923

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