ClinVar Miner

Submissions for variant NM_001349338.3(FOXP1):c.*4029del

dbSNP: rs753706183
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000368060 SCV000446030 uncertain significance Intellectual Disability with Language Impairment and Autistic Features 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003437100 SCV004150471 benign not provided 2022-05-01 criteria provided, single submitter clinical testing FOXP1: BS1, BS2

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.