List of variants reported as uncertain significance for Familial hypokalemia-hypomagnesemia by MGZ Medical Genetics Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.1145C>T (p.Thr382Met)	rs187885782	0.00006
NM_001126108.2(SLC12A3):c.457G>A (p.Val153Met)	rs779074538	0.00004
NM_001126108.2(SLC12A3):c.1049C>T (p.Ser350Leu)	rs778585043	0.00002
NM_001126108.2(SLC12A3):c.671C>A (p.Ala224Asp)	rs1437937060

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