List of variants reported as benign for Leber congenital amaurosis 19 by Genome-Nilou Lab

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: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001346022.3(USP45):c.2333A>G (p.Asn778Ser)	rs6570065	0.98245
NM_001346022.3(USP45):c.378-9C>T	rs6934692	0.84824
NM_001346022.3(USP45):c.1710A>G (p.Gly570=)	rs4504482	0.28479
NM_001346022.3(USP45):c.1562G>C (p.Arg521Thr)	rs41288947	0.26453
NM_001346022.3(USP45):c.199A>G (p.Lys67Glu)	rs7744845	0.23995
NM_001346022.3(USP45):c.1309-26_1309-22del	rs66817403

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.