List of variants reported as likely benign for Morquio syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000485.2(APRT):c.-50C>A	rs8191469	0.06915
NM_000485.3(APRT):c.*3A>G	rs2070256	0.05786
NM_000512.5(GALNS):c.*524G>C	rs3759946	0.04660
NM_000512.5(GALNS):c.*296A>G	rs79507351	0.02153
NM_000485.3(APRT):c.97C>T (p.Leu33=)	rs8191473	0.01977
NM_000485.3(APRT):c.*47T>C	rs8191497	0.01906
NM_000512.5(GALNS):c.*224C>G	rs111233947	0.01437
NM_000485.3(APRT):c.90G>T (p.Ser30=)	rs8191472	0.01050
NM_000485.3(APRT):c.*182A>G	rs8191498	0.00599

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.