Variants in gene SETD2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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_014159.7(SETD2):c.2251C>A (p.Pro751Thr)	rs115788094	0.00034
NM_014159.7(SETD2):c.5900G>A (p.Gly1967Asp)	rs143991928	0.00031
NM_014159.7(SETD2):c.3484C>T (p.His1162Tyr)	rs137871492	0.00028
NM_014159.7(SETD2):c.5829C>G (p.Asn1943Lys)	rs369421455	0.00006
NM_014159.7(SETD2):c.3026T>C (p.Met1009Thr)	rs114527197	0.00005
NM_014159.7(SETD2):c.2819G>T (p.Gly940Val)	rs751707090	0.00001
NM_014159.7(SETD2):c.6029C>T (p.Thr2010Ile)	rs2041416610	0.00001
NM_014159.7(SETD2):c.6970G>T (p.Ala2324Ser)	rs1162711197

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.