List of variants in gene CHD7 reported as benign by Athena Diagnostics Inc

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_017780.4(CHD7):c.6103+8C>T	rs3763592	0.14641
NM_017780.4(CHD7):c.6276G>A (p.Glu2092=)	rs2068096	0.12528
NM_017780.4(CHD7):c.7356A>G (p.Thr2452=)	rs2272727	0.04082
NM_017780.4(CHD7):c.6135G>A (p.Pro2045=)	rs6999971	0.03071
NM_017780.4(CHD7):c.6738G>A (p.Glu2246=)	rs61729627	0.01533
NM_017780.4(CHD7):c.307T>A (p.Ser103Thr)	rs41272435	0.01358
NM_017780.4(CHD7):c.6111C>T (p.Pro2037=)	rs41312170	0.00625
NM_017780.4(CHD7):c.6282A>G (p.Gly2094=)	rs41312172	0.00354
NM_017780.4(CHD7):c.7209G>A (p.Arg2403=)	rs61746518	0.00255
NM_017780.4(CHD7):c.1536A>G (p.Pro512=)	rs148577619	0.00218
NM_017780.4(CHD7):c.216T>C (p.Tyr72=)	rs16926453	0.00217
NM_017780.4(CHD7):c.2751G>A (p.Thr917=)	rs369429961	0.00040
NM_017780.4(CHD7):c.5697C>G (p.Gly1899=)	rs528130317	0.00004

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.