List of variants in gene combination LOC126862361, SLC12A3 reported as uncertain significance for Familial hypokalemia-hypomagnesemia

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: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.2930T>C (p.Leu977Ser)	rs201696394	0.00016
NM_001126108.2(SLC12A3):c.*18C>G	rs2289112	0.00008
NM_001126108.2(SLC12A3):c.2954G>A (p.Cys985Tyr)	rs199849117	0.00008
NM_001126108.2(SLC12A3):c.2963C>T (p.Ser988Leu)	rs141867836	0.00004
NM_001126108.2(SLC12A3):c.2987C>A (p.Thr996Asn)	rs201058248	0.00004
NM_001126108.2(SLC12A3):c.*102T>C	rs886052159	0.00001
NM_001126108.2(SLC12A3):c.*53A>G	rs1388199048	0.00001
NM_001126108.2(SLC12A3):c.3062A>G (p.Gln1021Arg)	rs762026283	0.00001
NM_001126108.2(SLC12A3):c.*209T>A	rs886052160
NM_001126108.2(SLC12A3):c.2925-33A>G	rs1567452700
NM_001126108.2(SLC12A3):c.2925-3C>T
NM_001126108.2(SLC12A3):c.2937A>T (p.Ile979=)	rs1596964738
NM_001126108.2(SLC12A3):c.2969A>G (p.Tyr990Cys)
NM_001126108.2(SLC12A3):c.2972T>C (p.Met991Thr)	rs1210754569
NM_001126108.2(SLC12A3):c.2984A>C (p.Glu995Ala)
NM_001126108.2(SLC12A3):c.3010C>T (p.Pro1004Ser)
NM_001126108.2(SLC12A3):c.3056A>G (p.Tyr1019Cys)	rs572393663

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.