List of variants in gene STAT3 reported as likely benign by GeneDx

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.550+210A>C	rs35162488	0.20465
NM_139276.3(STAT3):c.550+190C>A	rs62075768	0.03709
NM_139276.3(STAT3):c.550+230A>C	rs76487950	0.02064
NM_139276.3(STAT3):c.550+250C>A	rs868518205	0.01757
NM_139276.3(STAT3):c.273+263G>A	rs112232969	0.01443
NM_139276.3(STAT3):c.2144+74T>C	rs45540033	0.01386
NM_139276.3(STAT3):c.1888+205A>G	rs17879962	0.01383
NM_139276.3(STAT3):c.2102-79G>A	rs17885291	0.01319
NM_139276.3(STAT3):c.274-128C>G	rs17884756	0.01123
NM_139276.3(STAT3):c.797+156C>A	rs17881759	0.00714
NM_139276.3(STAT3):c.128+64T>C	rs17882334	0.00702
NM_139276.3(STAT3):c.2257+31A>G	rs114401618	0.00559
NM_139276.3(STAT3):c.551-84C>A	rs113751085	0.00285
NM_139276.3(STAT3):c.1329C>T (p.Thr443=)	rs147955721	0.00091
NM_139276.3(STAT3):c.225G>A (p.Ser75=)	rs146184566	0.00089
NM_139276.3(STAT3):c.273+22A>G	rs2291282	0.00035
NM_139276.3(STAT3):c.2288C>T (p.Ser763Leu)	rs140604473	0.00014
NM_139276.3(STAT3):c.2228G>T (p.Gly743Val)	rs151033214	0.00011
NM_139276.3(STAT3):c.373-4G>C	rs376611360	0.00010
NM_139276.3(STAT3):c.2091T>A (p.Ala697=)	rs200529713	0.00006
NM_139276.3(STAT3):c.1233+20C>T	rs761232183
NM_139276.3(STAT3):c.1281+11T>C	rs776564054
NM_139276.3(STAT3):c.1365+143_1365+146del	rs143987966
NM_139276.3(STAT3):c.1365+146dup	rs143987966
NM_139276.3(STAT3):c.1600+11C>T	rs1204881810
NM_139276.3(STAT3):c.1888+6G>A	rs1555563842
NM_139276.3(STAT3):c.273+145T>C	rs117120730
NM_139276.3(STAT3):c.468+58del	rs397712608
NM_139276.3(STAT3):c.551-57_551-18del	rs768181932
NM_139276.3(STAT3):c.551-77ATTCCCTCAGGTCAAGGAGT[2]	rs768181932
NM_139276.3(STAT3):c.551-84_551-25del
STAT3:c.1601-72_1601-71del	rs149538586
STAT3:c.469-34_469-30del	rs140846959

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