List of variants reported as benign for Hypermanganesemia with dystonia, polycythemia, and cirrhosis

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_018713.3(SLC30A10):c.*744G>T	rs2275707	0.85264
NM_018713.3(SLC30A10):c.*276C>T	rs138571819	0.02157
NM_018713.3(SLC30A10):c.-54C>A	rs115645353	0.01743
NM_018713.3(SLC30A10):c.640+10G>A	rs79328219	0.00931
NM_018713.3(SLC30A10):c.516C>G (p.Gly172=)	rs539271108	0.00006
NM_018713.3(SLC30A10):c.*1088G>A	rs2275706
NM_018713.3(SLC30A10):c.*1128del	rs59755757
NM_018713.3(SLC30A10):c.*115C>G	rs2231736

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.