ClinVar Miner

Submissions for variant NM_001009999.3(KDM1A):c.1072+3A>G

dbSNP: rs1553129313
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
GeneDx RCV001722614 SCV000716363 likely benign not provided 2018-04-30 criteria provided, single submitter clinical testing
GenomeConnect, ClinGen RCV000845019 SCV000986852 not provided Neurodevelopmental and congenital anomalies no assertion provided phenotyping only Variant interpretted as Uncertain significance and reported on 04/10/2018 by GTR ID Illumina Clinical Services Laboratory. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.

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.