Variants in gene STAT3 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.551-4G>A	rs80162032	0.00115
NM_139276.3(STAT3):c.1329C>T (p.Thr443=)	rs147955721	0.00091
NM_139276.3(STAT3):c.825T>G (p.Leu275=)	rs200098006	0.00023
NM_139276.3(STAT3):c.405C>T (p.Ala135=)	rs201846078	0.00008
NM_139276.3(STAT3):c.1365+143_1365+146del	rs143987966
NM_139276.3(STAT3):c.1365+146dup	rs143987966
NM_139276.3(STAT3):c.468+58del	rs397712608
STAT3:c.469-34_469-30del	rs140846959

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.