ClinVar Miner

List of variants reported as pathogenic for canthal anomaly by Genomic Research Center, Shahid Beheshti University of Medical Sciences

Included ClinVar conditions (57):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP
NM_001163817.2(DHCR7):c.1A>G (p.Met1Val) rs104886033
NM_002834.5(PTPN11):c.174C>G (p.Asn58Lys) rs397507506
NM_005633.3(SOS1):c.1655G>A (p.Arg552Lys) rs397517154
NM_023067.4(FOXL2):c.843_859dup (p.Pro287fs) rs672601359

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.