List of variants in gene NLGN3 reported as benign by Ambry Genetics

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: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_181303.2(NLGN3):c.2250C>T (p.Ala750=)	rs5981083	0.01113
NM_181303.2(NLGN3):c.1954A>G (p.Thr652Ala)	rs144914894	0.00197
NM_181303.2(NLGN3):c.807C>T (p.Ser269=)	rs151276700	0.00064
NM_181303.2(NLGN3):c.2370C>T (p.Pro790=)	rs372131545	0.00025
NM_181303.2(NLGN3):c.10C>T (p.Arg4Trp)	rs376877146	0.00009
NM_181303.2(NLGN3):c.2040C>T (p.Asn680=)

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.