ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.5090A>G (p.Asp1697Gly) (rs375761808)

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
Centre for Mendelian Genomics,University Medical Centre Ljubljana RCV000626891 SCV000747594 likely pathogenic Congenital cerebellar hypoplasia; Seizures; Absent speech; Microcephaly; Periventricular leukomalacia; Severe global developmental delay 2017-01-01 criteria provided, single submitter clinical testing
Centre for Mendelian Genomics,University Medical Centre Ljubljana RCV001197118 SCV001367754 uncertain significance Mental retardation, autosomal dominant 14 2018-12-13 criteria provided, single submitter clinical testing This variant was classified as: Uncertain significance. The available evidence on this variant's pathogenicity is insufficient or conflicting. The following ACMG criteria were applied in classifying this variant: PP3,PP5.

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.