List of variants reported as likely benign for Mucopolysaccharidosis type 6 by Illumina Laboratory Services, Illumina

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000046.3(ARSB):c.-564A>G	rs59558132	0.16591
NM_000046.3(ARSB):c.-958A>G	rs57586329	0.15967
NM_000046.3(ARSB):c.-906C>G	rs62377914	0.14171
NM_000046.3(ARSB):c.*3195A>G	rs16875887	0.07068
NM_000046.5(ARSB):c.98C>T (p.Ala33Val)	rs201168448	0.01022
NM_000046.5(ARSB):c.317G>A (p.Arg106His)	rs150087888	0.00230
NM_000046.5(ARSB):c.*2243A>G	rs145585943	0.00069
NM_000046.5(ARSB):c.313-12T>C	rs574816959	0.00001
NM_000046.4(ARSB):c.-322dup	rs11424557
NM_000046.4(ARSB):c.-410_-407delCTAA	rs151289643

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.