List of variants reported as pathogenic for Liddle syndrome by OMIM

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001039.4(SCNN1G):c.1589A>G (p.Asn530Ser)	rs148985177	0.00069
NM_001038.6(SCNN1A):c.1435T>C (p.Cys479Arg)	rs201873521	0.00016
NM_000336.3(SCNN1B):c.1696C>T (p.Arg566Ter)	rs137852704	0.00001
NM_000336.3(SCNN1B):c.1735_1766del (p.Ala579Leufs*4)	rs2142050610
NM_000336.3(SCNN1B):c.1847C>G (p.Pro616Arg)	rs387906402
NM_000336.3(SCNN1B):c.1847C>T (p.Pro616Leu)	rs387906402
NM_000336.3(SCNN1B):c.1849C>T (p.Pro617Ser)	rs137852708
NM_000336.3(SCNN1B):c.1858T>C (p.Tyr620His)	rs137852707
NM_001039.4(SCNN1G):c.1699C>T (p.Gln567Ter)	rs2141946607
NM_001039.4(SCNN1G):c.1718G>A (p.Trp573Ter)	rs137853342
NM_001039.4(SCNN1G):c.1749_1753del (p.Glu583fs)	rs1567270184
SCNN1B, 1-BP INS, 592C

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