List of variants in gene STAT3 reported as pathogenic for autoimmune disease

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: 16

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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.1032G>C (p.Gln344His)	rs869312887
NM_139276.3(STAT3):c.1057G>T (p.Val353Phe)	rs869312891
NM_139276.3(STAT3):c.1144C>T (p.Arg382Trp)	rs113994135
NM_139276.3(STAT3):c.1175A>G (p.Lys392Arg)	rs587777648
NM_139276.3(STAT3):c.1243G>A (p.Glu415Lys)	rs193922717
NM_139276.3(STAT3):c.1260T>G (p.Asn420Lys)	rs869312893
NM_139276.3(STAT3):c.1261G>A (p.Gly421Arg)	rs869312888
NM_139276.3(STAT3):c.1938C>G (p.Asn646Lys)	rs587777649
NM_139276.3(STAT3):c.1974G>C (p.Lys658Asn)	rs587777650
NM_139276.3(STAT3):c.1988C>T (p.Thr663Ile)	rs869312889
NM_139276.3(STAT3):c.2107G>A (p.Ala703Thr)	rs869312894
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.551-1G>C	rs1598423756

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