ClinVar Miner

List of variants in gene ORC6 reported as pathogenic for Meier-Gorlin syndrome 3

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_014321.4(ORC6):c.1A>G (p.Met1Val) rs777153067
NM_014321.4(ORC6):c.257_258del (p.Ser85_Phe86insTer) rs786205258
NM_014321.4(ORC6):c.2T>C (p.Met1Thr) rs146795505
NM_014321.4(ORC6):c.449+5G>A rs572314014
NM_014321.4(ORC6):c.598_601AGAA[1] (p.Lys201fs) rs879255692
NM_014321.4(ORC6):c.695A>C (p.Tyr232Ser) rs387906969

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.