ClinVar Miner

Submissions for variant NM_001184880.2(PCDH19):c.1569C>T (p.His523=)

gnomAD frequency: 0.00001  dbSNP: rs753119035
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001703824 SCV000524147 likely benign not provided 2019-03-04 criteria provided, single submitter clinical testing
Ambry Genetics RCV002318434 SCV000851052 likely benign Inborn genetic diseases 2016-06-10 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Labcorp Genetics (formerly Invitae), Labcorp RCV002525365 SCV003451503 likely benign Developmental and epileptic encephalopathy, 9 2023-08-30 criteria provided, single submitter clinical testing

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.