ClinVar Miner

List of variants in gene combination CFAP298, SYNJ1 reported as uncertain significance for Early-onset Parkinson disease 20; Developmental and epileptic encephalopathy, 53

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NC_000021.8:g.(?_33974153)_(34100371_?)dup
NC_000021.9:g.(?_32601843)_(32634904_?)dup

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.