ClinVar Miner

List of variants reported as likely benign for childhood malignant neoplasm by KCCC/NGS Laboratory, Kuwait Cancer Control Center

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_177438.3(DICER1):c.3269+14G>A rs201906274 0.00040
NM_177438.3(DICER1):c.1329C>T (p.Cys443=) rs776143079 0.00004
NM_177438.3(DICER1):c.4899A>G (p.Val1633=) rs878855271 0.00003
NM_177438.3(DICER1):c.4796G>A (p.Arg1599Gln) rs569615549 0.00002
NM_177438.3(DICER1):c.2553G>A (p.Gln851=) rs373715574 0.00001
NM_177438.3(DICER1):c.2718C>T (p.Arg906=) rs370692165 0.00001
NM_177438.3(DICER1):c.2613C>T (p.Asp871=) rs759827733
NM_177438.3(DICER1):c.4807C>T (p.Leu1603=) rs201320420

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.