List of variants in gene STAT3 reported as likely pathogenic for 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: 27

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.1003C>T (p.Arg335Trp)	rs193922716
NM_139276.3(STAT3):c.1022C>T (p.Thr341Ile)	rs1131691377
NM_139276.3(STAT3):c.1110-1G>A	rs1598406651
NM_139276.3(STAT3):c.1165A>G (p.Thr389Ala)	rs2081905517
NM_139276.3(STAT3):c.1177G>T (p.Val393Leu)	rs2144773766
NM_139276.3(STAT3):c.1235C>T (p.Thr412Ile)
NM_139276.3(STAT3):c.1255G>A (p.Gly419Arg)	rs1555565595
NM_139276.3(STAT3):c.1261G>A (p.Gly421Arg)	rs869312888
NM_139276.3(STAT3):c.1397A>C (p.Asn466Thr)	rs1057521091
NM_139276.3(STAT3):c.1414A>G (p.Asn472Asp)	rs1057520377
NM_139276.3(STAT3):c.1744G>A (p.Glu582Lys)	rs1064796762
NM_139276.3(STAT3):c.1843A>G (p.Lys615Glu)	rs1598393453
NM_139276.3(STAT3):c.1846G>C (p.Glu616Gln)	rs1064794899
NM_139276.3(STAT3):c.1863C>A (p.Phe621Leu)	rs1555563854
NM_139276.3(STAT3):c.1868G>T (p.Trp623Leu)	rs786205503
NM_139276.3(STAT3):c.1943T>A (p.Met648Lys)	rs1064796922
NM_139276.3(STAT3):c.1969_1971delinsCAG (p.Tyr657Gln)	rs1064794421
NM_139276.3(STAT3):c.1979T>C (p.Met660Thr)	rs886039434
NM_139276.3(STAT3):c.1988C>T (p.Thr663Ile)	rs869312889
NM_139276.3(STAT3):c.2117T>C (p.Leu706Pro)	rs1131691476
NM_139276.3(STAT3):c.2125A>G (p.Lys709Glu)	rs1555562364
NM_139276.3(STAT3):c.2131A>G (p.Ile711Val)	rs1131691937
NM_139276.3(STAT3):c.2144+1G>A	rs2144622620
NM_139276.3(STAT3):c.475G>A (p.Glu159Lys)	rs1555568535
NM_139276.3(STAT3):c.551-1G>A	rs1598423756
NM_139276.3(STAT3):c.919dup (p.Glu307fs)
NM_139276.3(STAT3):c.992T>G (p.Met331Arg)	rs1085307931

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