ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.977A>G (p.Asn326Ser)

gnomAD frequency: 0.00001  dbSNP: rs2499502460
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002376773 SCV002689441 uncertain significance Inborn genetic diseases 2024-02-26 criteria provided, single submitter clinical testing The p.N326S variant (also known as c.977A>G), located in coding exon 9 of the LRRK2 gene, results from an A to G substitution at nucleotide position 977. The asparagine at codon 326 is replaced by serine, an amino acid with highly similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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.