List of variants reported as likely pathogenic for Familial hypokalemia-hypomagnesemia by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.1926-1G>T	rs755560627	0.00001
NM_001126108.2(SLC12A3):c.2555G>A (p.Arg852His)	rs751929135	0.00001
NC_000016.9:g.(?_56899118)_56906295del
NM_000203.5(IDUA):c.1868T>C (p.Leu623Pro)	rs2153023287
NM_000339.2:c.(?_-30)_885del
NM_001126108.2(SLC12A3):c.1188C>A (p.Cys396Ter)	rs747139582
NM_001126108.2(SLC12A3):c.1262G>A (p.Cys421Tyr)	rs781342495
NM_001126108.2(SLC12A3):c.1850A>G (p.Gln617Arg)
NM_001126108.2(SLC12A3):c.2186G>C (p.Gly729Ala)
NM_001126108.2(SLC12A3):c.2369-2A>G
NM_001126108.2(SLC12A3):c.2800C>T (p.Arg934Trp)

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