List of variants reported as benign for corneal disorder by Willoughby Group, Queen's University Belfast

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001367624.2(ZNF469):c.9555C>G (p.Ala3185=)	rs273585636	0.00052
NM_001367624.2(ZNF469):c.1020C>T (p.Gly340=)	rs273585633	0.00022
NM_001367624.2(ZNF469):c.1627G>A (p.Gly543Ser)	rs281865145	0.00009
NM_001367624.2(ZNF469):c.10573G>A (p.Glu3525Lys)	rs273585628	0.00001
NM_001367624.2(ZNF469):c.6091G>A (p.Glu2031Lys)	rs273585622	0.00001
NM_001367624.2(ZNF469):c.2643C>G (p.Ser881=)	rs273585635
NM_001367624.2(ZNF469):c.3320G>A (p.Arg1107Gln)	rs281865148
NM_001367624.2(ZNF469):c.4910G>C (p.Arg1637Pro)	rs273585621

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.