ClinVar Miner

List of variants reported as benign for Familial hypokalemia-hypomagnesemia by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.2755C>T (p.Arg919Cys)	rs12708965	0.03475
NM_001126108.2(SLC12A3):c.2182G>A (p.Ala728Thr)	rs36049418	0.01075

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