ClinVar Miner

Submissions for variant NM_002894.3(RBBP8):c.298C>T (p.Arg100Trp) (rs373804633)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Developmental Genetics Unit,King Faisal Specialist Hospital & Research Centre RCV000115043 SCV000108551 pathogenic Seckel syndrome 2 no assertion criteria provided research
OMIM RCV000115043 SCV000150114 pathogenic Seckel syndrome 2 2014-02-01 no assertion criteria provided literature only

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.