List of variants in gene NLGN4X reported as uncertain significance for autism, susceptiblity to

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_181332.3(NLGN4X):c.2360C>T (p.Thr787Met)	rs4995611	0.00016
NM_181332.3(NLGN4X):c.2084C>T (p.Ala695Val)	rs1200279731	0.00001
NM_181332.3(NLGN4X):c.2294G>A (p.Arg765His)	rs1323836608	0.00001
NM_181332.3(NLGN4X):c.1309C>T (p.Arg437Trp)
NM_181332.3(NLGN4X):c.1614A>C (p.Gln538His)
NM_181332.3(NLGN4X):c.1661T>C (p.Phe554Ser)	rs1601840441
NM_181332.3(NLGN4X):c.187C>A (p.Pro63Thr)	rs150566193
NM_181332.3(NLGN4X):c.2080G>A (p.Ala694Thr)	rs2031290322
NM_181332.3(NLGN4X):c.2259G>C (p.Arg753Ser)	rs886042929
NM_181332.3(NLGN4X):c.2428G>A (p.Gly810Arg)	rs1181689310
NM_181332.3(NLGN4X):c.872A>G (p.Tyr291Cys)	rs2032034964

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.