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

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.2221G>A (p.Gly741Arg)	rs138977195	0.00041
NM_001126108.2(SLC12A3):c.1928C>T (p.Pro643Leu)	rs140012781	0.00014
NM_001126108.2(SLC12A3):c.2554C>T (p.Arg852Cys)	rs373899077	0.00011
NM_001126108.2(SLC12A3):c.1315G>A (p.Gly439Ser)	rs759377924	0.00009
NM_001126108.2(SLC12A3):c.179C>T (p.Thr60Met)	rs371443644	0.00004
NM_001126108.2(SLC12A3):c.1925G>A (p.Arg642His)	rs147901432	0.00003
NM_001126108.2(SLC12A3):c.2546T>A (p.Leu849His)	rs185927948	0.00001

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