ClinVar Miner

List of variants in gene NLGN3 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
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.603C>G (p.Pro201=) rs35794236 0.00055
NM_181303.2(NLGN3):c.594T>C (p.Gly198=) rs144247281 0.00053
NM_181303.2(NLGN3):c.21G>A (p.Pro7=) rs372993497 0.00014
NM_181303.2(NLGN3):c.435C>T (p.Asn145=) rs771275997 0.00011
NM_181303.2(NLGN3):c.10C>T (p.Arg4Trp) rs376877146 0.00009
NM_181303.2(NLGN3):c.2166C>T (p.Asn722=) rs146992370 0.00003
NM_181303.2(NLGN3):c.1473C>T (p.Ala491=) rs747037180 0.00002
NM_181303.2(NLGN3):c.1703+5G>T rs746912425 0.00002
NM_181303.2(NLGN3):c.870T>C (p.Gly290=) rs1400594230 0.00001
NM_181303.2(NLGN3):c.2243G>A (p.Arg748Gln) rs748757954
NM_181303.2(NLGN3):c.2331C>T (p.Ala777=) rs759656254
NM_181303.2(NLGN3):c.652A>C (p.Met218Leu) rs797045793
NM_181303.2(NLGN3):c.981A>G (p.Pro327=) rs797045794

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.