List of variants in gene SLC26A2 reported as uncertain significance by Natera, Inc.

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: 21

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000112.4(SLC26A2):c.782C>G (p.Ser261Cys)	rs114260147	0.00075
NM_000112.4(SLC26A2):c.1046T>A (p.Phe349Tyr)	rs114212275	0.00073
NM_000112.4(SLC26A2):c.1081G>A (p.Ala361Thr)	rs139051143	0.00026
NM_000112.4(SLC26A2):c.1512G>A (p.Met504Ile)	rs76668544	0.00022
NM_000112.4(SLC26A2):c.474T>C (p.Arg158=)	rs374572095	0.00014
NM_000112.4(SLC26A2):c.1744C>T (p.Arg582Cys)	rs142542254	0.00011
NM_000112.4(SLC26A2):c.704C>T (p.Ala235Val)	rs777906405	0.00009
NM_000112.4(SLC26A2):c.172C>T (p.Arg58Cys)	rs369318758	0.00003
NM_000112.4(SLC26A2):c.2164T>C (p.Ser722Pro)	rs565149029	0.00003
NM_000112.4(SLC26A2):c.645T>C (p.Ser215=)	rs1396953137	0.00003
NM_000112.4(SLC26A2):c.712T>G (p.Phe238Val)	rs746734591	0.00002
NM_000112.4(SLC26A2):c.740A>G (p.Tyr247Cys)	rs768745973	0.00002
NM_000112.4(SLC26A2):c.1057C>T (p.His353Tyr)	rs758078719	0.00001
NM_000112.4(SLC26A2):c.1427A>G (p.Tyr476Cys)	rs145765282	0.00001
NM_000112.4(SLC26A2):c.502C>T (p.Leu168=)	rs745566850	0.00001
NM_000112.4(SLC26A2):c.533G>A (p.Arg178Gln)	rs747117439	0.00001
NM_000112.4(SLC26A2):c.709G>A (p.Gly237Ser)	rs758186195	0.00001
NM_000112.4(SLC26A2):c.1634G>A (p.Arg545His)	rs745802790
NM_000112.4(SLC26A2):c.225GAA[1] (p.Lys76del)	rs1204857377
NM_000112.4(SLC26A2):c.892C>A (p.His298Asn)	rs1025069199
NM_000112.4(SLC26A2):c.902A>G (p.Asn301Ser)	rs750646790

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.