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

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.1928C>T (p.Pro643Leu)	rs140012781	0.00014
NM_001126108.2(SLC12A3):c.2186G>T (p.Gly729Val)	rs373901523	0.00008
NM_001126108.2(SLC12A3):c.1443+1G>A
NM_001126108.2(SLC12A3):c.1924C>G (p.Arg642Gly)	rs200697179
NM_001126108.2(SLC12A3):c.2659C>T (p.Arg887Ter)	rs747383768

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