ClinVar Miner

List of variants reported as pathogenic for Rahman syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP
NM_005321.2(H1-4):c.425_426insG rs1131690805
NM_005321.2(H1-4):c.436_458del (p.Thr146fs) rs1131690807
NM_005321.2(H1-4):c.441dupC rs1131690806

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.