List of variants reported as uncertain significance for Familial hypokalemia-hypomagnesemia; Bartter syndrome by Sydney Genome Diagnostics, Children's Hospital Westmead

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.1964G>A (p.Arg655His)	rs121909380	0.00011
NM_000338.3(SLC12A1):c.1942G>A (p.Asp648Asn)	rs137853157	0.00006
NM_000338.3(SLC12A1):c.610G>T (p.Val204Phe)	rs1442023118	0.00001
NM_000338.3(SLC12A1):c.1970C>T (p.Ala657Val)	rs2041701051
NM_000388.4(CASR):c.2710G>C (p.Gly904Arg)	rs2074943924
NM_001126108.2(SLC12A3):c.1378G>A (p.Gly460Ser)	rs2055210264
NM_001126108.2(SLC12A3):c.1486G>T (p.Gly496Cys)	rs777612082
NM_001126108.2(SLC12A3):c.2207A>T (p.Asn736Ile)	rs1424832490
NM_001126108.2(SLC12A3):c.427A>G (p.Met143Val)	rs1964378547

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