ClinVar Miner

List of variants reported as pathogenic for Feingold syndrome by GeneReviews

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
Download table as spreadsheet
NM_005378.6(MYCN):c.1103_1104AG[3] (p.Ser369fs)
NM_005378.6(MYCN):c.1117C>T (p.Arg373Ter) rs754137452
NM_005378.6(MYCN):c.1178G>A (p.Arg393His) rs104893646
NM_005378.6(MYCN):c.1181G>A (p.Arg394His) rs104893648
NM_005378.6(MYCN):c.964C>T (p.Arg322Ter) rs759103701

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.