List of variants reported as likely pathogenic for Familial hypokalemia-hypomagnesemia by Natera, Inc.

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.961C>T (p.Arg321Trp)	rs150046661	0.00011
NM_001126108.2(SLC12A3):c.1145C>T (p.Thr382Met)	rs187885782	0.00006
NM_001126108.2(SLC12A3):c.1390G>A (p.Ala464Thr)	rs201945662	0.00006
NM_001126108.2(SLC12A3):c.248G>A (p.Arg83Gln)	rs768527231	0.00004
NM_001126108.2(SLC12A3):c.434G>A (p.Arg145His)	rs374324018	0.00004
NM_001126108.2(SLC12A3):c.938C>T (p.Ala313Val)	rs140551719	0.00004
NM_001126108.2(SLC12A3):c.2721-1G>A	rs761242621	0.00002
NM_001126108.2(SLC12A3):c.1046C>T (p.Pro349Leu)	rs121909383	0.00001
NM_001126108.2(SLC12A3):c.2660G>A (p.Arg887Gln)	rs369360334	0.00001
NM_001126108.2(SLC12A3):c.1096-2A>G	rs2055189357
NM_001126108.2(SLC12A3):c.1196G>T (p.Arg399Leu)	rs13306668
NM_001126108.2(SLC12A3):c.1763C>T (p.Ala588Val)	rs121909382
NM_001126108.2(SLC12A3):c.268C>T (p.His90Tyr)	rs1596883431
NM_001126108.2(SLC12A3):c.547_548dup (p.Ile184fs)	rs770513014

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