List of variants reported as likely pathogenic for Pseudohypoaldosteronism, type IB1, autosomal recessive; Bronchiectasis with or without elevated sweat chloride 2; Liddle syndrome 3

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001038.6(SCNN1A):c.1435T>C (p.Cys479Arg)	rs201873521	0.00016
NM_001038.6(SCNN1A):c.1439+1G>A	rs1369791519
NM_001038.6(SCNN1A):c.1522C>T (p.Arg508Ter)	rs137852634
NM_001038.6(SCNN1A):c.685-1G>A
NM_001038.6(SCNN1A):c.69del (p.Asn24fs)	rs1565488675
NM_001038.6(SCNN1A):c.979+1G>A
NM_001038.6(SCNN1A):c.979G>T (p.Gly327Cys)

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