List of variants reported as uncertain significance for Liddle syndrome 3 by Fulgent Genetics, Fulgent Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001038.6(SCNN1A):c.1426C>T (p.Arg476Trp)	rs113622727	0.00020
NM_001038.6(SCNN1A):c.997C>T (p.Arg333Cys)	rs146177203	0.00010
NM_001038.6(SCNN1A):c.385G>A (p.Ala129Thr)	rs141756749	0.00006
NM_001038.6(SCNN1A):c.1177G>A (p.Asp393Asn)	rs886049758	0.00003
NM_001038.6(SCNN1A):c.319G>A (p.Gly107Arg)	rs144763378	0.00002
NM_001038.6(SCNN1A):c.457A>T (p.Ile153Phe)	rs775335440	0.00002
NM_001038.6(SCNN1A):c.777C>G (p.Ile259Met)	rs866913999	0.00001
NM_001038.6(SCNN1A):c.-54-13G>A	rs573341191
NM_001038.6(SCNN1A):c.1361G>A (p.Gly454Glu)	rs72657557

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