ClinVar Miner

List of variants reported as uncertain significance for Primary hyperoxaluria, type III by Clinical Biochemistry Laboratory,Health Services Laboratory

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_138413.4(HOGA1):c.212-21A>G rs11817730
NM_138413.4(HOGA1):c.341-82del rs796052083
NM_138413.4(HOGA1):c.396G>A (p.Ala132=) rs41290456
NM_138413.4(HOGA1):c.469-13C>T rs750664684
NM_138413.4(HOGA1):c.469-25C>T rs7078003
NM_138413.4(HOGA1):c.469-31C>T rs75929214
NM_138413.4(HOGA1):c.700+67G>A rs2297643
NM_138413.4(HOGA1):c.701-18G>C rs201596675
NM_138413.4(HOGA1):c.745C>G (p.Gln249Glu) rs368276974
NM_138413.4(HOGA1):c.834+42G>T rs115279832
NM_138413.4(HOGA1):c.912C>A (p.Ala304=) rs12261752

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.