List of variants reported as pathogenic for Familial hyperaldosteronism type II by OMIM

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004366.6(CLCN2):c.515G>A (p.Arg172Gln)	rs1293789661	0.00001
CLCN2, LYS362DEL
NM_004366.6(CLCN2):c.2593A>C (p.Ser865Arg)	rs1553853557
NM_004366.6(CLCN2):c.65T>A (p.Met22Lys)	rs758379595
NM_004366.6(CLCN2):c.71G>A (p.Gly24Asp)	rs1085307938
NM_004366.6(CLCN2):c.76T>A (p.Tyr26Asn)	rs1553857113

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