ClinVar Miner

List of variants studied for Congenital anomalies of kidney and urinary tract type 2 by OMIM

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP
NM_001080508.3(TBX18):c.1010del (p.Gly337fs) rs869320679
NM_001080508.3(TBX18):c.1570C>T (p.His524Tyr) rs760905589
NM_001080508.3(TBX18):c.487A>G (p.Lys163Glu) rs797045022

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.