List of variants reported as likely pathogenic for Familial hypokalemia-hypomagnesemia by Illumina Laboratory Services, Illumina

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.363G>C (p.Glu121Asp)	rs146632606	0.00102
NM_001126108.2(SLC12A3):c.1946C>T (p.Thr649Met)	rs145337602	0.00009
NM_001126108.2(SLC12A3):c.1390G>A (p.Ala464Thr)	rs201945662	0.00006
NM_001126108.2(SLC12A3):c.2863C>T (p.Arg955Trp)	rs559626481	0.00006
NM_001126108.2(SLC12A3):c.1387G>A (p.Gly463Arg)	rs374163823	0.00004
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.247C>T (p.Arg83Trp)	rs201255508	0.00003

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