List of variants in gene SLC30A10 reported as uncertain significance by GeneDx

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

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_018713.3(SLC30A10):c.1293C>A (p.His431Gln)	rs79106013	0.00074
NM_018713.3(SLC30A10):c.284C>T (p.Thr95Ile)	rs188273166	0.00060
NM_018713.3(SLC30A10):c.269C>T (p.Thr90Ile)	rs554675480	0.00019
NM_018713.3(SLC30A10):c.1118C>A (p.Ala373Glu)	rs202111121	0.00009
NM_018713.3(SLC30A10):c.1270C>T (p.His424Tyr)	rs375331656	0.00006
NM_018713.3(SLC30A10):c.1180A>G (p.Lys394Glu)	rs1207616870	0.00002
NM_018713.3(SLC30A10):c.1009A>G (p.Ile337Val)	rs773025168	0.00001
NM_018713.3(SLC30A10):c.1207C>T (p.Pro403Ser)	rs1659520346	0.00001
NM_018713.3(SLC30A10):c.1455T>A (p.Phe485Leu)
NM_018713.3(SLC30A10):c.167G>C (p.Ser56Thr)	rs1241483390
NM_018713.3(SLC30A10):c.194C>T (p.Thr65Ile)	rs377636913
NM_018713.3(SLC30A10):c.85G>A (p.Gly29Ser)

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.