List of variants reported as pathogenic for Familial hypokalemia-hypomagnesemia by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.2864G>A (p.Arg955Gln)	rs202114767	0.00008
NM_001126108.2(SLC12A3):c.626G>A (p.Arg209Gln)	rs758035631	0.00004
NM_001126108.2(SLC12A3):c.1195C>T (p.Arg399Cys)	rs775931992	0.00002

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