ClinVar Miner

List of variants reported as uncertain significance for Familial hyperaldosteronism type II

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004366.6(CLCN2):c.1934G>A (p.Arg645Gln)	rs375401465	0.00007
NM_004366.6(CLCN2):c.1912G>A (p.Ala638Thr)
NM_004366.6(CLCN2):c.482G>C (p.Gly161Ala)

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