ClinVar Miner

List of variants reported as likely pathogenic by Department of Internal Medicine, University of Texas Health Science Center at Houston

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP
NM_001256071.3(RNF213):c.12037G>A (p.Asp4013Asn) rs397514563
NM_001256071.3(RNF213):c.12343_12345del (p.Lys4115del) rs797045187
NM_001256071.3(RNF213):c.14429G>A (p.Arg4810Lys) rs112735431

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.