ClinVar Miner

Submissions for variant GRCh38/hg38 5q15(chr5:97712762-97763616)x1

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
Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu RCV000225312 SCV000212305 benign Premature ovarian failure 2015-01-07 criteria provided, single submitter reference population
Institute of Molecular and Cell Biology, University of Tartu RCV000161408 SCV000191365 not provided Large for gestational age no assertion provided case-control

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.