List of variants in gene SLC12A3 reported as benign 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: 26

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.791C>G (p.Ala264Gly)	rs1529927	0.97710
NM_001126108.2(SLC12A3):c.1670-8T>C	rs2304483	0.48985
NM_001126108.2(SLC12A3):c.1395C>T (p.Thr465=)	rs5801	0.15318
NM_001126108.2(SLC12A3):c.2521+278C>T	rs16963395	0.12416
NM_001126108.2(SLC12A3):c.2142C>T (p.Ala714=)	rs5803	0.11388
NM_001126108.2(SLC12A3):c.2598C>T (p.Gly866=)	rs5804	0.09125
NM_001126108.2(SLC12A3):c.2711G>A (p.Arg904Gln)	rs11643718	0.08381
NM_001126108.2(SLC12A3):c.1884G>A (p.Ser628=)	rs5802	0.08069
NM_001126108.2(SLC12A3):c.366A>G (p.Ala122=)	rs2304479	0.05592
NM_001126108.2(SLC12A3):c.1023C>T (p.Phe341=)	rs2229209	0.04172
NM_001126108.2(SLC12A3):c.1825+9C>A	rs35797045	0.03711
NM_001126108.2(SLC12A3):c.2755C>T (p.Arg919Cys)	rs12708965	0.03475
NM_001126108.2(SLC12A3):c.1865A>G (p.Asn622Ser)	rs61746763	0.01422
NM_001126108.2(SLC12A3):c.1567+290G>A	rs148931404	0.01145
NM_001126108.2(SLC12A3):c.2182G>A (p.Ala728Thr)	rs36049418	0.01075
NM_001126108.2(SLC12A3):c.1539C>T (p.Tyr513=)	rs146805986	0.00597
NM_001126108.2(SLC12A3):c.2857-6G>A	rs117981500	0.00557
NM_001126108.2(SLC12A3):c.774C>T (p.Asn258=)	rs111578437	0.00523
NM_001126108.2(SLC12A3):c.2083G>A (p.Gly695Arg)	rs36031476	0.00473
NM_001126108.2(SLC12A3):c.249G>T (p.Arg83=)	rs76750525	0.00433
NM_001126108.2(SLC12A3):c.965C>T (p.Ala322Val)	rs142679083	0.00157
NM_001126108.2(SLC12A3):c.1386C>T (p.Phe462=)	rs142199602	0.00048
NM_001126108.2(SLC12A3):c.1825+5G>A	rs368509876	0.00029
NM_001126108.2(SLC12A3):c.2368+8C>A	rs140236327	0.00015
NM_001126108.2(SLC12A3):c.1543A>G (p.Ile515Val)	rs554432544	0.00003
NM_001126108.2(SLC12A3):c.1176C>T (p.Thr392=)	rs117440321

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.