ClinVar Miner

List of variants in gene combination TP53, WRAP53 reported as likely benign for Cushing syndrome

Included ClinVar conditions (24):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP
NM_018081.2(WRAP53):c.-206G>A rs17551150
NM_018081.2(WRAP53):c.-245G>C rs17883670
NM_018081.2(WRAP53):c.31C>T (p.Pro11Ser) rs17880282
NM_018081.2(WRAP53):c.407C>G (p.Pro136Arg) rs34067256
NM_018081.2(WRAP53):c.450C>T (p.Phe150=) rs2287498

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.