ClinVar Miner

List of variants reported as likely pathogenic for Familial hypokalemia-hypomagnesemia by Institute of Immunology and Genetics Kaiserslautern

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.533C>T (p.Ser178Leu)	rs772589653	0.00001
NM_001126108.2(SLC12A3):c.947G>C (p.Gly316Ala)	rs748920885

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