List of variants in gene STAT3 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.2144+20C>T	rs8069115	0.03624
NM_139276.3(STAT3):c.1680C>T (p.Ser560=)	rs146817483	0.00145
NM_139276.3(STAT3):c.551-4G>A	rs80162032	0.00115
NM_139276.3(STAT3):c.1492A>G (p.Ile498Val)	rs146620441	0.00078
NM_139276.3(STAT3):c.825T>G (p.Leu275=)	rs200098006	0.00023
NM_139276.3(STAT3):c.2228G>T (p.Gly743Val)	rs151033214	0.00011
NM_139276.3(STAT3):c.804G>A (p.Thr268=)	rs755554248	0.00006
NM_139276.3(STAT3):c.1366-4G>A	rs373653543	0.00003
NM_139276.3(STAT3):c.1059C>T (p.Val353=)	rs774847480	0.00001
NM_139276.3(STAT3):c.2200T>C (p.Leu734=)	rs746221967	0.00001
NM_139276.3(STAT3):c.348A>G (p.Leu116=)	rs200960081	0.00001
NM_139276.3(STAT3):c.1018A>G (p.Lys340Glu)
NM_139276.3(STAT3):c.1392C>T (p.Ile464=)
NM_139276.3(STAT3):c.1601-10dup	rs3830585
NM_139276.3(STAT3):c.1756A>T (p.Met586Leu)
NM_139276.3(STAT3):c.2144C>T (p.Pro715Leu)	rs1064794957
NM_139276.3(STAT3):c.2153G>A (p.Cys718Tyr)
NM_139276.3(STAT3):c.274-8A>T	rs772586829

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