ClinVar Miner

List of variants in gene NLGN3 studied for autism, susceptibility to, X-linked 1

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_181303.2(NLGN3):c.913+11C>G rs202038845 0.00018
NM_181303.2(NLGN3):c.1384G>A (p.Ala462Thr)
NM_181303.2(NLGN3):c.1411C>T (p.Arg471Cys) rs121917893
NM_181303.2(NLGN3):c.163C>T (p.Arg55Ter)
NM_181303.2(NLGN3):c.1672A>G (p.Met558Val) rs2147908798
NM_181303.2(NLGN3):c.1685C>T (p.Thr562Ile)
NM_181303.2(NLGN3):c.2222T>G (p.Leu741Arg)
NM_181303.2(NLGN3):c.2342A>G (p.His781Arg)
NM_181303.2(NLGN3):c.611T>C (p.Val204Ala)
NM_181303.2(NLGN3):c.707A>G (p.Asn236Ser) rs2092405042
NM_181303.2(NLGN3):c.806G>A (p.Ser269Asn) rs2092439435
NM_181303.2(NLGN3):c.913+1G>A rs2147900685

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.